INIS 10-K
Radnostix Inc (INIS)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
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DOCUMENTS INCORPORATED BY REFERENCE
Certain information called for in Part III of this Annual Report on Form 10-K is incorporated by reference from the registrant’s definitive proxy statement for the 2022 annual meeting of shareholders, which will be filed with the Securities and Exchange Commission not later than 120 days after the registrant’s fiscal year ended December 31, 2021.
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INTERNATIONAL ISOTOPES INC.
FORM 10-K
TABLE OF CONTENTS
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Cautionary Note Regarding Forward-Looking Statements
This Annual Report on Form 10-K (the “Annual Report”) contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including statements regarding industry prospects and future results of operations or financial position, made in this Annual Report are forward-looking. Words such as: “anticipates,” “believes,” “should,” “expects,” “future” and “intends” and similar expressions identify forward-looking statements. In particular, statements regarding: financial condition, operating results and liquidity, future cash flow from operations, our ability to achieve profitability, the status of our proposed uranium de-conversion facility, the expected growth in business segment revenues, our expansion into new markets, the ability of our products to compete with several larger companies and products, the results of market studies used to support our business model, our anticipated improvement in economic conditions, the expected increased revenue resulting from sales of our U.S. Food and Drug Administration (FDA)-approved sodium iodide product, our ability to continue cobalt-60 production, and the sufficiency of our available cash and revenues from operations to meet our operating needs, are forward-looking. Forward-looking statements reflect management’s current expectations, plans or projections and are inherently uncertain. Actual results could differ materially from management's expectations, plans or projections. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this Annual Report. Certain risks and uncertainties that could cause actual results to differ significantly from management’s expectations are described in the section entitled “Risk Factors” in this Annual Report. That section, along with other sections of this Annual Report, describes some, but not all, of the factors that could cause actual results to differ significantly from management’s expectations. We do not intend to publicly release any revisions to these forward-looking statements that may be made to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. Readers are urged, however, to review the risks and other factors set forth in the other reports that we file from time to time with the Securities and Exchange Commission (the “SEC”).
PART I
| Item 1. | BUSINESS |
General Business and Products Description
International Isotopes Inc. (the “Company”, “we”, “us” and “our”) produces an FDA approved generic sodium iodide I-131 drug product, manufactures a wide range of nuclear medicine calibration and reference standards, and provides radiochemicals for clinical research and life sciences. The Company also produces a variety of cobalt-60 products and supports contract manufacturing activities for clients radiopharmaceutical and radiochemical products.
We were formed as a Texas corporation in 1995. Our wholly-owned subsidiaries are International Isotopes Idaho Inc., a Texas corporation; International Isotopes Fluorine Products, Inc., an Idaho corporation; International Isotopes Transportation Services, Inc., an Idaho corporation; RadQual, LLC, a [X] limited liability company (RadQual); and TI Services, LLC, a [X] limited liability company (TI Services). Our core business consists of five reportable segments which include: Nuclear Medicine Standards, Cobalt Products, Radiochemical Products, Radiological Services, and Fluorine Products.
During 2021, we focused our efforts on achieving profitability in each of our core business segments and reached several significant goals. During 2021, we:
| Ÿ | Increased sales in the Radiochemical segment by 5% mainly due to a 9% increase in sales of our FDA approved generic sodium iodide I-131 drug product. |
| Ÿ | Purchased the remaining 75.5% of RadQual for an aggregate purchase price of approximately $4.4 million, which was paid in shares of our common stock, resulting in the issuance of 40,176,236 shares of our common stock as consideration, making RadQual and TI Services wholly owned subsidiaries of International Isotopes, Inc. |
| Ÿ | Successfully obtained cobalt-60 from the Department of Energy (DOE) to increase our cobalt source production activities which contributed to an 11% increase in Cobalt Product revenues. |
| Ÿ | Developed several new products for our Nuclear Medicine products segment and expanded these products into Positron Emission Tomography (PET) imaging standards. |
| Ÿ | Expanded sales of our nuclear medicine products through exercising our management opportunity with RadQual, LLC (RadQual). In particular, we increased our international sales by utilizing the marketing and distribution expertise of our wholly owned subsidiary TI Services; and |
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| Ÿ | Continued to pursue viable opportunities to obtain government or commercial contracts for depleted uranium de-conversion services for our U.S. Nuclear Regulatory Commission (NRC) licensed de-conversion project in Lea County, New Mexico. |
Also, in February 2022, we completed the previously announced sale of certain assets (the “Assets”) to Pharmalogic Idaho, LLC for $4.0 million in cash (the “Transaction”) pursuant to the terms of the Asset Purchase Agreement, dated February 10, 2022 (the “Agreement”). The Assets consisted primarily of manufacturing equipment and a sublease acquired by the Company in connection with the previously announced termination of the manufacturing and supply agreement with another company.
In 2022, we plan to continue efforts to further expand and improve upon our operations in our core business segments. We intend to continue to invest in these segments and work to pursue product development, reduce production costs, and expand sales in each of our segments. The following paragraphs provide a brief description of each of our business segments. Certain financial information with respect to each of our business segments, including revenues from external customers, a measure of profit or loss, and total assets, is set forth in Note 15 to our Consolidated Financial Statements which begin on page F-7.
Nuclear Medicine Standards
This segment consists of the manufacture of sources and standards associated with Single Photon Emission Computed Tomography (SPECT) and Positron Emission Tomography (PET) imaging, patient positioning, and calibration or operational testing of dose measuring equipment for the nuclear pharmacy industry. Our nuclear medicine standards products include flood sources, dose calibrators, rod sources, flexible and rigid rulers, spot markers, pen point markers, and a host of specialty design items. These products are manufactured through an exclusive manufacturing agreement with our wholly-owned subsidiary, RadQual. In July 2021, we purchased the remaining 75.5% interest of RadQual. Prior this purchase we were one of two managing members of RadQual and had significant influence in management decisions with regard to RadQual’s business operations. Following the July 2021 acquisition, we have now fully consolidated the income and expenses from both RadQual LLC and TI Services.
There are over 5,000 nuclear medicine centers in the United States (U.S.) that require nuclear medicine products on a regular repeat basis. We have been manufacturing these products for RadQual since 2001. Most nuclear medicine product sales are to U.S. customers. However, in recent years, because of stronger marketing efforts, we have seen an increase in foreign sales, as shown in Note 14 to the accompanying audited financial statements. All these products contain radioactive isotopes that decay at a predictable rate. Therefore, customers are required to periodically replace most of these products when they reach the end of their useful lives. The useful life of these products varies depending on the isotope used in manufacture, but in most cases averages eighteen months to two years. Most of the isotopes used in manufacturing these nuclear medicine products are available from various sources world-wide and we are not dependent on a single supplier. In addition to the products themselves, we have developed a complete line of specialty packaging for the safe transportation and handling of these products.
Cobalt Products
Our cobalt products segment includes the production of bulk cobalt (cobalt-60), fabrication of cobalt capsules for radiation therapy as well as various industrial applications, and recycling of expended cobalt sources.
Bulk cobalt sales have historically accounted for a significant amount of the total revenue from this business segment, and we are reliant on cobalt production in the DOE’s Advanced Test Reactor (ATR) located in Idaho. Through continued work with the DOE, a new cobalt target was designed and in October 2014 we entered into a ten-year agreement with the DOE for the irradiation of the new target design. In 2020 and 2021, we received shipments of these cobalt targets. Unfortunately, their specific activity was far below expectations. As such, we revised our contract with the DOE to purchase the remainder of these cobalt targets at a discounted rate. We are again working with the DOE to schedule future production of both high and low specific activity cobalt. After completing the 2014 agreement with the DOE, we entered into contracts with several customers for the sale of this material. In accordance with those agreements, we began receiving pre-payments from customers on future cobalt shipments which we recorded as unearned revenue. We were able to fulfill some of these contracts with the cobalt we received in 2020 and 2021 from the ATR and with cobalt we obtained through secondary suppliers. Accordingly, at the time of shipment, customer payments previously recorded as deferred revenue were reclassified as revenue.
The year-over-year demand for cobalt products has remained strong as a result of the introduction of several new types of cobalt therapy units and we have continued to see demand for cobalt-manufactured products for those devices. We have explored, and intend to continue to explore, opportunities to further develop cobalt products and sales on an on-going basis. The production, use, transport, and import/export of these products are all heavily regulated, but we have developed an experienced staff of technicians, shipping specialists, and supervisors as part of our efforts to comply with the regulations and support cost effective, timely delivery of these products.
At the present time, we are the sole purchaser of high activity cobalt from any of the DOE reactors in the U.S. There are a few other cobalt source manufacturers in North America. We believe both our product and service provide us with a competitive edge in competing with these other manufacturers.
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Radiochemical Products
This segment includes the production and distribution of various isotopically pure radiochemicals for medical, industrial, and research applications. These products are either directly produced by us or are purchased in bulk from other producers and distributed by us in customized packages and chemical forms tailored to meet customer and market demands. In February 2020, we received FDA approval of our ANDA for our generic sodium iodide I-131 drug product. Our generic sodium iodide drug product is the only generic product of this type manufactured in the U.S. and offers customers an attractive domestic alternative to the single existing foreign commercial drug manufacturer. We have two suppliers of sodium iodide I-131 from whom we purchased material during 2021 to produce this product in the most reliable manner possible.
In April 2019, we entered into a manufacturing and supply agreement with a company to provide contract manufacturing services for certain iodine products. We completed a 6,000 square foot expansion to our existing facility and installed the equipment necessary to support this cGMP contract manufacturing opportunity. However, in December 2020, at the request of the other company we terminated the contract manufacturing relationship through a settlement agreement. As part of the agreement, we received a termination payment consisting of cash and the other company’s relinquishment on all claims to their improvements in the expansion to our facility and all the equipment purchased by them. The termination payment resulted in a significant one-time gain of approximately $2,900,000 which we recognized under “other income” in 2020. In February 2022, we were able to sell these improvements and equipment in the expansion of our facility for an additional gain of approximately $1,800,000.
Radiological Services
The current services included in this segment are radioactive source disposal and processing certain materials for exempt distribution.
On May 2, 2019, our radiological services team was involved in a contamination event involving a breached cesium-137 source at an off-site location in the state of Washington. This work was being performed under a contract with the DOE. On January 5, 2021, we were notified by the DOE that we had been indemnified from any financial liability for this event under the Price Anderson Act (PAA). As part of this indemnification notification, we received payment in full for our claim with the DOE for recovery of certain expenses incurred for this event. We recognized Other Income of approximately $150,000 in the 2021, for additional cost recoveries for this event. All remaining cost recoveries as part of this settlement with the DOE were recognized in previous financial periods pursuant to ASC 410-30. We used these funds to pay all outstanding subcontractors and reimburse their insurance company for payments they previously paid to us for this matter. We concluded a final settlement with our insurance company and all others regarding this claim in 2021.
Our corrective actions for this event included termination of all field service activities and removal of these activities from the Company’s NRC license. The loss in revenue resulting from suspension of radiological field service work has been compensated for by increased revenues in our remaining business segments.
In January 2020 we notified our gemstone processing customer that we were terminating their contract for a failure to meet minimum processing volume requirements. The termination activities and wrap up of this service was substantially concluded in 2021 and we saw a steady decline in revenue from this service as production has been concluding. In the first half of 2022, we plan to convert the spaces in the facility that had been used to perform this contract work into expanded Nuclear Medicine product manufacturing. The loss in revenue expected from termination of the gemstone processing agreement is expected to be more than compensated for by the expansion of sales in our nuclear medicine and radiochemical products segments.
Fluorine Products and the Planned Uranium De-Conversion Facility
We established the fluorine products business segment in 2004 to support production and sale of various fluoride gases produced using our Fluorine Extraction Process (FEP). FEP was intended to be completed in conjunction with the operation of a proposed depleted uranium (DUF6) de-conversion facility in Lea County, New Mexico. DUF6 is the waste by-product of uranium enrichment, and any uranium enrichment facility will create very large quantities of DUF6. In October 2012, we received a construction and operating license from the NRC for the planned facility. Changes in the nuclear industry near the end of 2013, however, significantly reduced commercial demand for this type of facility. Therefore, we suspended all further development work on the project. We still anticipate a potential future need for a depleted uranium conversion facility and, therefore, we are keeping all licenses and permits current.
In connection with the proposed de-conversion facility, Lea County, New Mexico transferred property to us under the provisions of the New Mexico Local Economic Development Act, Project Participation Agreement (PPA) as a location for construction of the facility. Under the original agreement, we were obligated to meet certain performance objectives for construction start and staffing levels. Because of the project delay we did not meet those objectives. We plan to continue to work with Lea County to execute a modification to the agreement at some future point should the project move forward. If we do not extend or modify the commitment
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dates in a modified agreement then we may either purchase or re-convey the property to Lea County, New Mexico. If we do not retain title to the property, it could have a material adverse impact on future plans for the project.
Industry Overview, Target Markets, and Competition
The industries and markets that require or involve the use of radioactive material are diverse. Our current core business operations involve products that are used in a wide variety of applications and in various markets. The following provides an explanation of the markets and competitive factors affecting our current business segments.
Nuclear Medicine Standards
Calibration and reference standards are required for the daily operational checks and calibration of the measurement of SPECT and PET imaging devices frequently used in nuclear medicine. Calibration and quality assurance testing are required as a routine part of the normal operations of this equipment to ensure its reliability and accuracy. We exclusively manufacture many of these reference standard products for our wholly-owned subsidiary, RadQual, which in turn has many distributors who make direct sales in the U.S. and internationally. We directly ship these products to all 50 states and many overseas locations. There is only one other major producer of these products in the world that competes directly with us for these products. Most of the products manufactured by our competitor are similar in design to our products because all must meet Original Equipment Manufacturer (OEM) dimensional and performance standards. However, we attempt to differentiate our products from our competitor’s products through increased levels of quality control and customer service. We are certified under ISO-9001:2015 and ISO-13485-2016 quality programs that have allowed us to start selling these products into several foreign countries that require this additional quality certification for manufacturers. We use a small number of suppliers for the isotopes and other materials used in manufacturing these nuclear medicine products, but if we were to lose any of these suppliers, others would be available. We are also working to expand the number and types of products that are manufactured in this segment.
Cobalt Products
In 2014, we entered into a new 10-year agreement with the DOE utilizing a new cobalt target design for high activity cobalt production. Because of the lengthy irradiation time required we initially anticipated that cobalt shipments to customers would resume in late 2018. However, due to delays in the ATR operating schedule we were not able to take our first shipment of these targets until March 2020. Due to lower than desired activity rates in the material, we bought the remaining targets at a discounted rate and are now working with the DOE on future purchases. Our cobalt products are used in applications such as radiation therapy, security devices, radiography examination and in some commercial applications. While there are other technologies available to provide external radiation therapy, there are several new devices just gaining market approval that still depend on cobalt sources for their specialized applications. There are currently no other producers of high specific activity cobalt in the U.S., however, there are producers of high specific activity material in Canada and several other countries. In addition to us, there is only one other company in the U.S. currently licensed to handle large quantities of cobalt.
There has been a significant increase in regulation by the NRC in recent years that has created a significant barrier to new entrants to this market. We expect steady demand for cobalt sealed source products over the next several years but are primarily dependent upon our contract relationship with the DOE for a large portion of our cobalt production supply. An interruption in the operation of the ATR could have a negative impact on our cobalt products business segment.
Radiochemical Products
In February 2020, our ANDA for a generic radiochemical sodium iodide drug product was approved by the FDA. This product is approved for use in treatment of hyperthyroidism and carcinoma of the thyroid and is the first and only generic sodium iodide I-131 product approved by the FDA in the US. Our product is the only generic product of this type manufactured in the U.S. The only other supplier in the U.S. of an FDA approved sodium iodide product comes from a foreign manufacturer.
We started commercial sales of the drug product in the first quarter of 2020, and these sales had a significant positive impact on our revenues for 2020 and 2021. We expect continued growth in sales for this product in 2022 and beyond. We are also considering other generic drug opportunities and plan to expand the range of FDA approved products offered within this business segment in the coming years.
We also supply radiochemical products in bulk form. The markets for most radiochemicals are highly competitive. The target markets for these products are customers who (1) incorporate them into finished industrial or medical devices; (2) use radioisotope products in clinical trials for various medical applications; or (3) further process and include the radioisotope products into pharmaceutical products approved by the U.S. FDA for labeled use in therapy or imaging.
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In February 2022, we sold the improvements and equipment in our expansion to our manufacturing facility. Using the capital from this sale, we are currently developing a business plan and exploring other opportunities to produce additional radiopharmaceutical products or explore new contract manufacturing opportunities. We believe that we are uniquely qualified and have a competitive advantage for future opportunities because we have a unique combination of NRC licensing, GMP compliant operating facility, and trained personnel.
Fluorine Products and the Planned Depleted Uranium De-Conversion Facility
Our Fluorine Products segment was developed in conjunction with uranium de-conversion to take advantage of the anticipated need for depleted uranium de-conversion services. During 2013, we curtailed all further work on the de-conversion facility because of a lack of demand for uranium de-conversion services at that time. However, we believe that in the future there will be a demand for this service to address still growing stockpiles of depleted UF6. When that demand occurs, we believe the groundwork we have completed on the depleted uranium de-conversion and fluorine extraction project should put us in a strong position to take advantage of the NRC license that has already been issued for this facility and should serve to justify the financial investment in this uranium de-conversion project in the future.
Radiological Services
In previous years, we performed radiological field service activities involving installation or decommissioning of radiation devices in hospitals, research institutions, and various other commercial facilities. In May 2019, while performing a contract for the DOE, our field services team was involved in a contamination event involving a breached cesium-137 source at an off-site location in the state of Washington. Because of the severity of this event, we suspended these contract activities and have removed this activity from our NRC license. We believe that the loss in revenue resulting from suspension of radiological field service work will be compensated for by increased revenues in our remaining business segments.
In January 2020 we notified our gemstone processing customer that the service contract with them was being terminated because the volume of gemstones sent for processing did not meet contract minimums. The termination activities and wrap up of this service were substantially performed in 2021 and we saw a steady decline in revenue from this service as production was wrapped up. In the first half of 2022, we plan to convert the spaces in the facility that were used to perform this contract work into increased Nuclear Medicine product manufacturing. The loss in revenue expected from termination of the gemstone processing agreement is expected to be more than compensated for by the expansion of new nuclear medicine source products.
Government Regulation
Licensing
We currently operate under two NRC licenses, one for broad scope operations and another for exempt distribution. Our broad scope license covers calibration and reference standard manufacturing and distribution, radioisotope processing and distribution, large scale cobalt processing and recycle operations, radioactive gemstone processing, environmental sample analysis, certain field service activities, and research and development. The exempt distribution license permits the release and distribution of irradiated gemstones to unlicensed entities in the U.S. All of our existing licenses and permits are adequate to allow current business operations. We do not handle “special nuclear materials” (i.e. nuclear fuels and weapons grade uranium, thorium or plutonium); therefore, our facility is not designated as a “nuclear” facility that would require additional licensing.
As a condition of our NRC licenses in Idaho, we are required to provide financial assurance for decommissioning activities. We fulfill this license requirement with a surety bond which names the NRC as beneficiary and is supported by a restricted cash account held in trust by a third party. Similar financial assurances will be required to fund the decommissioning of the proposed de-conversion facility.
In October 2012, we were granted a 40-year construction and operating license by the NRC for our planned depleted uranium de-conversion and fluorine extraction processing facility (the “de-conversion facility”). The de-conversion facility is planned to be located in Lea County, New Mexico. Further engineering work on the proposed de-conversion facility was placed on hold in 2013 until additional contracts for utilization could be obtained. There is no specific timeline required by the NRC for the start of construction on this project. The majority of the pre-construction design, licensing and state permitting has already been completed for the project and a ground water permit from the state of New Mexico remains to be obtained before the plant could begin operation.
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Regulation of Radioisotope Production Waste
All our manufacturing processes generate some radioactive waste. We must handle this waste pursuant to the Low-Level Radioactive Waste (LLRW) Policy Act (LLRW Act), which requires the safe disposal of mildly radioactive materials. The estimated costs for storage and disposal of these materials have been included in the manufacturing and sales price of our products. However, actual disposal costs are subject to change at the discretion of the disposal site and are ultimately applied at the time of disposal. We have obtained all necessary permits and approvals for the disposal of our waste materials, and we do not anticipate any negative changes in capacity or regulatory conditions that would limit or restrict our waste disposal capabilities.
Nuclear Regulatory Commission Oversight
We operate under two NRC licenses and are subject to NRC oversight and periodic inspections of our operations.
Other Regulations
We are registered as a medical device manufacturer through the FDA for several of our nuclear medicine reference and calibration standards. We are registered with the U.S. Department of Transportation (DOT) for the shipment of radioactive materials. We also have an NRC license for the import and export of radioactive materials. Because of increasing security controls and regulations, it is likely that we may encounter additional regulations affecting transportation, storage, sale, and import/export of radioactive materials.
We are also subject to inspection by the FDA to manufacture our sodium iodide I-131 product in compliance with our ANDA for sodium iodide I-131 and all applicable cGMP requirements for this and other contract manufactured products. We are registered with the FDA as a drug manufacturing facility, and we are subject to periodic and random inspections by the FDA for the continued manufacture of drug products.
We are subject to government regulation and intervention both in the U.S. and in all foreign jurisdictions in which we conduct business. Compliance with applicable laws and regulations results in higher capital expenditures and operating costs and changes to current regulations with which we must comply can necessitate further capital expenditures and increases in operating costs to enable continued compliance.
Environmental Compliance
We are subject to various federal, state, local and foreign government requirements regulating the discharge of materials into the environment or otherwise relating to the protection of the environment. These laws and regulations include, but are not limited to the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), the Resource Conservation and Recovery Act (RCRA) and state statutes such as the Idaho Hazardous Waste Management Act, the LLRW Policy Act, NRC regulations concerning various irradiated, radioactive, and depleted uranium materials, and U.S. DOT regulations concerning shipment of radioactive materials. Certain of these laws and regulations can impose substantial fines and criminal sanctions for violations and require installation of costly equipment or operational changes to limit emissions and/or decrease the likelihood of accidental hazardous substance releases. We have incurred, and expect to continue to incur, capital and operating costs to comply with these laws and regulations. For the years ended December 31, 2021 and 2020, we incurred costs of approximately $52,000 and $190,171, respectively, for licensing and monitoring fees. In addition, changes in laws, regulations and enforcement of policies, or the imposition of new clean-up requirements or remedial techniques, could require us to incur costs in the future that would have a negative effect on our financial condition or results of operations.
Distribution Methods for Products
We sell our products directly to our customers who, in some cases, are both end users and distributors. We use common commercial carriers for delivery of our products. For smaller quantities of material, and overnight and next-day delivery, we utilize other commercial carriers.
Dependence on Customers
Historically, we have been dependent on one customer, RadQual, of which we owned 24.5%, for a significant amount of our gross revenue. In July 2021, we purchased the remaining 75.5% of the ownership interest in RadQual, making it a wholly-owned subsidiary. Our sales to RadQual for 2021 accounted for approximately 28% of our total gross revenue for 2021 and our sales to RadQual for 2020 totaled approximately 26% of our total gross revenue for 2020. The change in ownership of RadQual has substantially eliminated any risks associated with having RadQual as a single major customer.
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Combined sales, on which we are dependent, to our three largest customers, accounted for 17% of our total gross revenues in 2021 and accounted for 11% of our total gross revenues in 2020.
Patents, Trademarks, Licenses and Royalty Agreements
In 2004, we obtained certain patents related to the FEP. In 2010, we were granted an additional process patent on the FEP process. During 2012, we were granted additional process patents for the FEP process in the United States.
Employees
As of December 31, 2021, we had 32 total employees, including 30 full-time employees.
Available Information
Our internet website address is www.intisoid.com. We are subject to the reporting requirements under the Securities Exchange Act of 1934, as amended (the Exchange Act). Consequently, we are required to file reports and information with the SEC, including Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K, and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act. These reports and other information concerning us are available free of charge through (i) our website as soon as reasonably practicable after they are electronically filed with, or furnished to, the SEC, and (ii) the SEC’s website at www.sec.gov. Information contained on, or accessible through, our website is not incorporated by reference into this Annual Report or other reports filed with the SEC.
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| Item 1A. | RISK FACTORS |
Readers should carefully consider the following factors that may affect our business, future operating results and financial condition, as well as other information included in this Annual Report. The risks and uncertainties described below are not the only ones the Company faces. Additional risks and uncertainties not presently known to us or that we currently deem immaterial also may impair our business operations. If any of the following risks occur, our business, financial condition and operating results could be materially adversely affected.
Risks Related To Our Company
We have incurred, and may continue to incur, losses. We have incurred net losses for most fiscal periods since our inception. From inception through December 31, 2021, we have generated $142,999,345 in revenues and an accumulated deficit (including preferred stock dividends and returns) in the amount of $126,764,081. The negative cash flow we have sustained has materially reduced our working capital, which in turn could materially and negatively impact our ability to fund future operations and continue to operate as a going concern. Management has taken and continues to take, actions to improve our financial condition and results of operations. The availability of necessary working capital, however, is subject to many factors beyond our control, including, among other things, our ability to obtain financing on favorable terms, or at all, economic cycles, market acceptance of our products, competitors' responses to our products, the intensity of competition in our markets, and the level of demand for our products.
We may need additional financing to continue operations. Because we may continue to experience negative cash flow, we may need to obtain additional financing to continue operations. Management will continue to plan and take actions to improve our financial results which could enhance our ability to obtain financing. However, obtaining additional financing is subject to many factors beyond our control and may not be available to us on acceptable terms or at all. If we are unable to raise additional funds when needed, we could be required to delay development and construction of projects, reduce the scope of, abandon or sell some or all our growth projects or default on our contractual commitments in the future, any of which would have a material adverse effect on our business, financial condition and operating results.
Our operations expose us to the risk of material environmental liabilities. We are subject to potential material liabilities related to the remediation of environmental hazards and to personal injuries or property damages that may be caused by hazardous substance releases and exposures. The materials used in our operations expose us to risks of environmental contamination that could subject us to liability, including remediation obligations that could be very costly. In addition, the discovery of previously unknown contamination could require us to incur costs in the future that would have a negative effect on our financial condition or results of operations. We have a Surety Bond in place supported by funds in a restricted cash account to provide the financial assurance required by the NRC for our Idaho facility license for decommissioning and a similar mechanism will be required to fund the decommissioning of the proposed new depleted uranium facility. However, if a contamination event occurred within, or outside of, our facility, we may be financially responsible to remediate such contamination and could have to borrow money or fund the remediation liability from our future revenue. We may not be able to borrow the funds, or have available revenue, sufficient to meet this potential liability, which could have a significant negative impact on our financial condition and results of operations.
We are dependent upon key personnel. Our ongoing operations are dependent on Steve T. Laflin, President and Chief Executive Officer. The loss of Mr. Laflin could have a material adverse effect on our business. There is no assurance that we will be able to retain Mr. Laflin or our existing personnel or attract additional qualified employees. The loss of any of our key personnel or an inability to attract additional qualified employees could result in a significant decline in revenue.
General economic conditions in markets in which we do business can impact the demand for our goods and services. Decreased demand for our products and services can have a negative impact on our financial performance and cash flow. Demand for our products and services, in part, depends on the general economic conditions affecting the countries and industries in which we do business. A downturn in economic conditions in the U.S. or industry that we serve may negatively impact demand for our products and services, in turn negatively impacting our operations and financial results. Further, changes in demand for our products and services can magnify the impact of economic cycles on our businesses.
Volatility in raw material and energy costs, interruption in ordinary sources of supply and an inability to recover unanticipated increases in energy and raw material costs from customers could result in lost sales or significantly increase the cost of doing business. Market and economic conditions affecting the costs of raw materials, utilities, energy costs, and infrastructure required for the delivery of our goods and services are beyond our control and any disruption or halt in supplies, or rapid escalations in costs could affect our ability to manufacture products or to competitively price our products in the marketplace. For instance, an interruption in the supply of isotopes such as cobalt-57, cobalt-60, or iodine-131 could result in lost sales of nuclear medicine and calibration standards sales, cobalt product sales, and sodium iodide I-131 generic drug product. We also purchase some of our radiochemical products from overseas suppliers and the price of those products could be adversely affected through changes in currency exchange rates.
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We are subject to extensive government regulation in jurisdictions around the globe in which we do business. Regulations address, among other things, environmental compliance, import/export restrictions, healthcare services, taxes and financial reporting, and can significantly increase the cost of doing business, which in turn can negatively impact our operations, financial results and cash flow. We are subject to government regulation and intervention both in the United States and in all foreign jurisdictions in which we conduct business. Compliance with applicable laws and regulations results in higher capital expenditures and operating costs and changes to current regulations with which we must comply can necessitate further capital expenditures and increases in operating costs to enable continued compliance. Additionally, from time to time, we may be involved in legal or administrative proceedings under certain of these laws and regulations. Significant areas of regulation and intervention include the following:
Radioactive Waste. All our manufacturing processes generate some radioactive waste. For waste that cannot be decayed in storage we must handle this waste pursuant to the LLRW Policy Act, which requires the safe disposal of mildly radioactive materials. The estimated costs for storage and disposal of these materials have been included in the manufacturing and sales price of our products. However, actual disposal costs are subject to change at the discretion of the disposal site and are ultimately applied at the time of disposal. An unexpected or material increase in these costs could have a material adverse effect on our financial condition and results of operations.
Health Compliance. Health regulations dictated by the United States Occupational Safety and Health Administration and NRC are extensive in our business. There is no assurance that our activities will comply with all applicable health regulations at times and, as a result, may expose us to liability under applicable health regulations. Costs and expenses resulting from such liability may materially negatively impact our operations and financial condition. Overall, health laws and regulations will continue to affect our business worldwide.
NRC License Enforcement Actions. The NRC may take enforcement action in the event that we are found to be in violation of NRC regulations or in violation of any of our license requirements. Consequences of violations depend upon the severity of the violations as well as the adequacy and timeliness of corrective actions implemented by the licensee to investigate and correct the cause of the violation and to prevent reoccurrence. The NRC has discretionary authority in the action they choose to take against license violations, but these actions can include civil penalties and restrictions upon licensee operations or license suspension. The imposition of any such penalties and/or restrictions upon our operations or suspension of our license could have a material adverse effect on our financial condition and results of operations.
Environmental Regulation. We are subject to various federal, state, local and foreign government requirements regulating the discharge of materials into the environment or otherwise relating to the protection of the environment. These laws and regulations include, but are not limited to CERCLA, the RCRA and state statutes such as the Idaho Hazardous Waste Management Act, the LLRW Policy Act, NRC regulations concerning various irradiated, radioactive, and depleted uranium materials, and U.S. DOT regulations concerning shipment of radioactive materials. Certain of these laws and regulations can impose substantial fines and criminal sanctions for violations and require installation of costly equipment or operational changes to limit emissions and/or decrease the likelihood of accidental hazardous substance releases. We have incurred, and expect to continue to incur, capital and operating costs to comply with these laws and regulations. In addition, changes in laws, regulations and enforcement of policies, or the imposition of new clean-up requirements or remedial techniques, could require us to incur costs in the future that would have a negative effect on our financial condition or results of operations.
Import/Export Regulation. We are subject to significant regulatory oversight of our import and export operations due to the nature of our product offerings. Penalties for non-compliance can be significant and violations can result in adverse publicity. Because of increasing security controls and regulations, it is likely that we may encounter additional regulations affecting the transportation, storage, sale, and import/export of radioactive materials.
Taxes. We structure our operations to be tax efficient and to make use of tax credits and other incentives. Nevertheless, changes in tax laws, actual results of operations, final audit of tax returns by taxing authorities, and the timing and rate at which tax credits can be utilized can change the rate at which we are taxed, thereby affecting our financial results and cash flow.
We may incur material losses and costs as a result of product liability claims that may be brought against us. We face an inherent business risk of exposure to product liability claims in the event that products supplied by us fail to perform as expected or such failures result, or are alleged to result, in bodily injury. Although we have purchased insurance with coverage and in amounts that we believe to be adequate and reasonable in light of our current and planned operations, including our planned uranium de-conversion and fluoride gas production business, if a successful product liability claim were brought against us in excess of our available insurance coverage, it would have a material adverse effect on our business and financial results.
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Catastrophic events such as natural disasters, pandemics, including the novel strain of coronavirus (COVID-19), war and acts of terrorism could disrupt our business or the business of our suppliers or customers, and any such disruptions could have a negative impact on our operations, financial results and cash flow. Our operations are at all times subject to the occurrence of catastrophic events outside our control, ranging from severe weather conditions such as hurricanes, floods, earthquakes and storms, to health epidemics and pandemics, to acts of war and terrorism. Any such event could cause a serious business disruption that could affect our ability to produce and distribute our products and possibly expose us to third-party liability claims. Additionally, such events could impact our suppliers, thereby causing energy and raw materials to become unavailable to us, and our customers, who may be unable to purchase or accept our products and services. Any such occurrence could have a negative impact on our operations and financial condition.
In addition, public health epidemics or outbreaks could adversely impact our business. For example, the COVID-19 pandemic had a significant impact upon our business operations in 2020 and 2021. The future developments of COVID-19, length and continued severity of the pandemic, the impacts of variants, the continued efficacy of vaccines, and the extent of further economic impact are highly uncertain and cannot be predicted with confidence. In particular, the continuation of the pandemic could result in a further negative impact on the global economy and financial markets, resulting in even more significant economic downturn, and could also continue to adversely impact our operations, including among others, our manufacturing and supply chain, sales and marketing and product development operations and could have a continued adverse impact on our operations, financial results, and cash flow.
As a result of the COVID-19 pandemic, we experienced a reduction of sales within our nuclear medicine calibration standards segment and radiochemicals segment during 2020 and 2021. There was no discernable impact from COVID-19 to our cobalt products business segment during the period. The decrease in sales for 2020 and 2021 for our nuclear medicine calibration standards segment was the result of the temporary closure of many imaging clinics and suspension of elective or non-essential imaging procedures.
To-date we have not furloughed or terminated any employees as a result of the financial impact of COVID-19. The Company has only seen a limited impact in our raw material supply chain related to the COVID-19, primarily some plastics which have been in strong demand for certain types of PPE. Alternative sources of raw materials have been obtained without any interruption to production. However, if we are unable to obtain alternative sources of raw materials in the future or if we experience other disruptions from the COVID-19 pandemic, we may experience an adverse impact on our operations, financial results, and cash flow.
Global economic and political conditions that affect supply chain fulfillment or create price inflation could have a negative effect on our operations and financial results. The raw materials we use for our products are shipped in from domestic or international suppliers. Global supply chain disruption can affect our ability to get these key raw materials. We ship our products throughout the United States and internationally. As such, increases to shipping costs due to inflated fuel costs or other relevant costs can affect the prices of our materials and shipping. These increased costs could have an adverse effect on our revenues and profit margins for our products.
Our future growth is largely dependent upon our ability to develop new products that achieve market acceptance with acceptable margins. Our businesses operate in global markets that are characterized by rapidly changing technologies and evolving industry standards. Accordingly, our future growth rate depends upon several factors, including, but not limited to, our ability to (i) identify emerging technological trends in our target end-markets, (ii) develop and maintain competitive products, (iii) enhance our products by adding innovative features that differentiate our products from those of our competitors, and (iv) develop, manufacture, and bring products to market quickly and cost-effectively. Our ability to develop new products based on technological innovation or U.S. FDA approval can affect our competitive position and requires the investment of significant resources. These development efforts divert resources from other potential investments in our businesses, and they may not lead to the development of new products on a timely basis or that meet the needs of our customers as fully as competitive offerings. In addition, the markets for our products may not develop or grow as we currently anticipate. The failure of our technologies or products to gain market acceptance due to more attractive offerings by our competitors could significantly reduce our revenues and adversely affect our competitive standing and prospects.
We are dependent on various third parties in connection with our business operations. The production of high-specific activity cobalt is dependent upon the DOE, and its prime-operating contractor, which controls the Idaho reactor. Current activity at the Idaho ATR may continue to affect the supply of cobalt material needed for the manufacture of cobalt sources. Loss of the ability to use, or cost-effectively use, these irradiation services would significantly impact our cobalt products business segment because there is not currently another reactor available in the U.S. that is capable of providing this type of service for us. Our radiochemical iodine is supplied to us through two supply sources. Unanticipated contract terminations by these suppliers or other third parties would have a material adverse impact on our operations, financial results, and cash flow.
We are dependent on a limited number of customers in connection with some of our current business operations. Combined sales to our three top customers accounted for 17% and 11% of our total gross revenue during 2021 and 2020, respectively. Although we are making efforts to reduce our dependency on a small number of customers, the loss of any one of these customers could have a significant impact on our future results of operations and financial condition. Unanticipated contract terminations by any of these current customers could have a material adverse impact on operations, financial results, and cash flow.
We are subject to competition from other companies. Each of our existing business areas has direct competition from other businesses. High-specific activity cobalt is supplied by other reactor facilities around the world. Nuclear medicine calibration and reference standards are being produced by one other major manufacturer in the U.S. We have one major competitor in the US for our sodium iodide I-131 drug product. Most of our radiochemicals are also manufactured by several other companies in the world, and there are other providers of radiological field services. Most of our competitors have significantly greater financial resources that could give them a competitive advantage over us.
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Risks Related To Our Common Stock
Trading in our common stock is limited and the price of our common stock may be subject to substantial volatility. Our common stock is quoted on the OTCQB Marketplace under the U.S. trading symbol “INIS”. The market for our securities is limited, the price of our stock is volatile, and the risk to investors in our common stock is greater than the risk associated with stock trading on other markets. These factors may reduce the potential market for our common stock by reducing the number of potential investors. This may make it more difficult for investors in our common stock to sell shares to third parties or to otherwise dispose of their shares. This could cause our stock price to decline.
We currently do not intend to pay dividends on our common stock. We do not plan to pay dividends on shares of our common stock in the near future. Consequently, an investor in our common stock can only achieve a return on its investment in us if the market price of our common stock appreciates.
We are contractually obligated to issue shares in the future, which will dilute your interest in us. As of December 31, 2021, there were approximately 15,507,500 shares of common stock issuable upon the exercise of vested stock options, at a weighted-average exercise price of $.05 per share. An additional 37,239,804 shares were reserved for issuance under our equity plans as of December 31, 2021. Our outstanding preferred stock and certain of our outstanding debt is also convertible into shares of our common stock at the holders’ option. In addition, we expect to issue additional options to purchase shares of our common stock to compensate employees, consultants and directors, and we may issue additional shares to raise capital to expand our manufacturing capability, develop additional products, or fund our planned uranium de-conversion plant. Any such issuances will have the effect of further diluting the interest of the holders of our securities. Also, outstanding as of December 31, 2021, were Class M Warrants (as defined below) for the issuance of 4,140,000 shares of common stock, which have since expired, and Class N Warrants (as defined below) for the issuance of 2,925,000 shares of common stock. The weighted average exercise price for all outstanding warrants as of December 31, 2021, was $0.11 per share. In February 2022, 515,000 Class M Warrants were exercised at a price of $0.12.
Risks Related to Our Proposed De-Conversion and FEP Produced Fluoride Gas Business
We will need to raise additional funds to complete the construction of our de-conversion and FEP facility. We need to secure more customer contracts and raise additional funds to complete the design and construction of a de-conversion facility with a production-scale FEP operation. We may not be able to raise the additional capital required to complete the facility on acceptable terms, or at all. In addition, the total funds required to complete this project have been based upon early preliminary estimates and, while we believe these estimates are conservative, unforeseen expenses may be incurred and additional funding may be required to complete the project.
We do not have an operating history with respect to our strategy to combine de-conversion services and FEP-produced fluoride gas products and this business may not succeed. We have no operating results with respect to providing de-conversion services or producing high volumes of fluoride gas products using FEP to date and, therefore, we do not have an operating history upon which you can evaluate this business or our prospects. Our prospects must be considered in light of the risks and uncertainties encountered in entering a new line of business.
Some of these risks relate to our potential inability to:
• construct our planned de-conversion and FEP production plant, including the effective management of the cost of the design and construction of the facility, and obtain the additional financing necessary for such construction;
• maintain the necessary regulatory approvals for the facility and the ongoing operations of the facility;
• obtain the groundwater permit from the state of New Mexico;
• produce commercially viable volumes of high-purity fluoride products using FEP;
• effectively manage this new business and its operations;
• successfully establish and maintain our intended low-cost structure; and
• successfully address the other risks described throughout this Annual Report.
If we cannot successfully manage these risks, our business and results of FEP operations and financial condition will suffer.
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There is no history of large-scale commercial fluoride gas production utilizing FEP. We have successfully demonstrated the feasibility of using FEP to produce some fluoride gases and Starmet Corporation (Starmet), which originally developed and patented the technology, also used FEP to produce a fluoride gas. However, FEP has not been used for large-scale commercial production of the size and magnitude envisioned in conjunction with the de-conversion process and there may be technical issues and process challenges related to the utilization of FEP for large-scale commercial production. Unforeseen issues associated with constructing and scaling up these new FEP operations could significantly impact our proposed schedule and our overall ability to produce high-purity fluoride gas in the quantities anticipated.
Prior to the start of operations of the facility, we must obtain a Ground Water Permit from the State of New Mexico, and we cannot guarantee the amount of time required to obtain this permit from the State of New Mexico for operation of these facilities. The operation of the planned depleted uranium de-conversion facility requires a ground water permit from the State of New Mexico. There is no assurance that the ground water permit will be issued to us by the State of New Mexico. We also have no control over the actual time required by the State of New Mexico to review and approve the application for the ground water permit. Failure to obtain the permit, or any delay in obtaining the permit, could delay the start of operations of our planned depleted uranium de-conversion facility, thereby delaying revenue-generating operations at the facility.
The DOE is obligated to take depleted uranium from enrichment companies. The DOE has constructed two depleted uranium de-conversion facilities. These facilities are obligated to process depleted uranium produced from United States commercial uranium enrichment facilities at a price determined by DOE. We believe our depleted uranium processing facility will offer the better value to enrichment companies, but we cannot assure you that enrichment companies will not select the DOE as their de-conversion service provider.
We may be handling large quantities of DUF6 and fluoride products, which are radioactive and hazardous materials, respectively, and are subject to intense regulation. The hazardous nature of DUF6 and fluoride products affects the actions we are required to take for licensing, air permitting, environmental review, emergency response, liability insurance, personnel training, and generally increases the level of concern by the general public with respect to our handling of these materials. All of these factors complicate the licensing and operations processes and involve a host of additional regulatory factors that could affect the timeline for completing our de-conversion and FEP facility. Additionally, the NRC is revising its regulations on the disposal of depleted uranium waste at LLRW disposal facilities that accept large quantities of depleted uranium. Any changes to the current regulations may result in increased disposal costs that we intend to pass through to our customers, which, depending on the significance of the increased cost, may cause potential customers to continue to store their DUF 6 rather than pay for de-conversion and disposal services.
We will be subject to competition from the DOE and other companies. While there are no currently operating commercial DUF6 de-conversion facilities in the U.S., the DOE is operating two de-conversion plants intended to process DUF6 from the DOE’s existing 1.5 billion-pound stockpile. Additionally, AREVA currently operates a de-conversion plant in France, Urenco is operating a conversion facility in the United Kingdom (U.K.), and the Russian State Atomic Energy Corporation ROSATOM has constructed a facility in Russia. We cannot assure you that the operators of the existing DUF 6 de-conversion facilities will not build additional facilities to expand their operations and compete with us in offering to provide de-conversion services or that commercial enrichment companies will not choose to ship their depleted DUF 6 overseas for processing in France, the U.K., or Russia.
We currently hold conditional title to the property in Lea County, New Mexico where the proposed plant is to be constructed. The property location for our planned facility is located in Lea County, New Mexico. Lea County, New Mexico has transferred the property to us under the provisions of the New Mexico Local Economic Development Act, Project Participation Agreement. Under the original agreement, we were obligated to meet certain performance objectives; namely starting Phase I construction no later than December 31, 2014, completing Phase I and hiring at least 75 employees by December 31, 2015, in order to retain title to the property. We did not meet either of those deadlines. However, in July 2015, we executed an amendment to the PPA that extended the due date of the Phase I construction to December 31, 2016, and Phase I completion and hiring at least 75 employees to December 31, 2016. We did not meet either of those deadlines. We plan to work with Lea County to execute an additional modification to the agreement to further extend these dates once an estimated restart date for the project is determined. If we do not succeed in extending the commitment dates then we may, at our sole option, either purchase or re-convey the property to Lea County, New Mexico. If Lea County does not agree to a contract modification and we do not retain title to the property, it could have a material adverse impact on our planned de-conversion and FEP project since another location would need to be selected and evaluated for environmental compliance.
| Item 1B. | UNRESOLVED STAFF COMMENTS |
We are a smaller reporting company, and therefore, are not required to provide the information required by this item.
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| Item 2. | PROPERTIES |
We lease one property which serves as or main corporate headquarters and houses all of our current manufacturing operations for our core business segments. We also hold the conditional title to 640 acres of land in Lea County, New Mexico for the proposed de-conversion facility. The following paragraphs provide a brief summary of these properties.
4137 Commerce Circle, Idaho Falls, Idaho – The facility located on this property houses our main corporate headquarters and all of our current manufacturing operations. In January 2020, we entered into a new lease agreement due to new and expanded facilities made available to us. The initial lease term is until January 2030 and provides an option to renew for an additional 5 years. The lease provides for the Company to expand its leased space as needed into additional areas of the building. The facility was new when leased in March 2001 and remains in excellent condition. We have a right of first refusal on this property that allows us to match any offer to purchase this property.
Land - Lea County, New Mexico – In August 2011, we received land from Lea County, New Mexico, pursuant to a PPA, whereby the land was deeded to us for no monetary consideration. In return, we committed to construct a uranium de-conversion and FEP facility on the land. In order to retain title to the property, we were to begin construction of the de-conversion facility no later than December 31, 2014, and complete Phase I of the project and have hired at least 75 persons to operate the facility no later than December 31, 2015, although commercial operations need not have begun by that date. We did not meet the performance milestones set forth in the PPA and we executed a modification to the agreement extending these due dates to December 31, 2016 and 2017, respectively. We plan to work with Lea County to execute an additional modification to the agreement to further extend these dates once an estimated restart date for the project is determined. If we do not succeed in extending the commitment dates or in reaching performance dates set forth in a modified agreement then we may, at our sole option, either purchase or re-convey the property to Lea County, New Mexico. The purchase price of the property would be $776,078, plus interest at the annual rate of 5.25% from the date of the closing to the date of payment. We have not recorded the value of this property as an asset and will not do so until such time that sufficient progress on the project has been made to meet our obligations under the agreements for permanent transfer of the title.
| Item 3. | LEGAL PROCEEDINGS |
We are not a party to any legal proceedings that we believe to be material and we are not aware of any pending or threatened litigation against us that we believe could have a material adverse effect on our business, operating results, financial condition, or cash flows.
| Item 4. | MINE SAFETY DISCLOSURES |
Not applicable.
PART II
| Item 5. | MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES |
Our common stock is traded on the OTCQB under the trading symbol “INIS”.
Holders of Record
As of March 22, 2021, there were 503 holders of record of our common stock.
Dividends
We have never paid any cash dividends on our common stock. In the future, and based upon our profit performance, our Board of Directors (the “Board”) will evaluate and determine whether to issue dividends, subject to compliance and limitations under any applicable debt or other financing agreements in effect at that time or retain funds for research and development and expansion of our business. We do not anticipate paying any dividends to shareholders of our common stock for the foreseeable future.
Recent Sales of Unregistered Securities; Use of Proceeds from Registered Securities
None.
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Purchases of Equity Securities by the Issuer
None.
Performance Graph
We are a smaller reporting company, and therefore, are not required to provide the information required by this item.
| Item 6. | [RESERVED] |
| Item 7. | MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS |
The following discussion of our results of operations and financial condition should be read in conjunction with the accompanying financial statements and related notes thereto included in Item 8, “Financial Statements and Supplementary Data,” within this Annual Report. Some of the information contained in this discussion and analysis or set forth elsewhere in this Annual Report, including information with respect to our plans and strategies for our business, statements regarding the industry outlook, our expectations regarding the future performance of our business and the other non-historical statements contained herein are forward-looking statements. See “Cautionary Note Regarding Forward-Looking Statements.” You should also review the “Risk Factors” in Item 1A. of this Annual Report for a discussion of important factors that could cause actual results to differ materially from the results described herein or implied by such forward-looking statements.
Overview
International Isotopes Inc. (the “Company”, “we”, “us” and “our”) produces an FDA approved generic sodium iodide I-131 drug product, manufactures a wide range of nuclear medicine calibration and reference standards and provides radiochemicals for clinical research and life sciences. The Company also produces a variety of cobalt-60 products and supports clients contract manufacturing of radiopharmaceutical and radiochemical products. A more detailed description of each of these product lines and services along with a description of our business segments can be found in Item 1, “Business” within this Annual Report.
During 2021, we focused our efforts on achieving profitability in each of our core business segments and reached several significant goals. During 2021, we:
| Ÿ | Increased sales in the Radiochemical segment by 5% mainly due to a 9% increase in sales of our FDA approved generic sodium iodide I-131 drug product. |
| Ÿ | Purchased the remaining 75.5% of RadQual, LLC, making RadQual, LLC and TI Services, LLC wholly-owned subsidiaries of International Isotopes, Inc. |
| Ÿ | Successfully obtained cobalt-60 from the Department of Energy (DOE) to increase our cobalt source production activities which contributed to an 11% increase in Cobalt Product revenues. |
| Ÿ | Developed several new products for our Nuclear Medicine products segment and expanded these products into Positron Emission Tomography (PET) imaging standards. |
| Ÿ | Expanded sales of our nuclear medicine products through exercising our management opportunity with RadQual, LLC (RadQual). In particular, increased our international sales by utilizing the marketing and distribution expertise of our joint venture with RadQual, TI Services, LLC (TI Services); and |
| Ÿ | Continued to pursue viable opportunities to obtain government or commercial contracts for depleted uranium de-conversion services for our U.S. Nuclear Regulatory Commission (NRC) licensed de-conversion project in Lea County, New Mexico. |
As a result of the COVID-19 pandemic, we experienced a reduction of sales within our nuclear medicine calibration standards segment and radiochemicals segment during 2020 and 2021. There was no discernable impact from COVID-19 to our cobalt products business segment during the period. The decrease in sales for 2020 and 2021 for our nuclear medicine calibration standards segment was the result of the temporary closure of many imaging clinics and suspension of elective or non-essential imaging procedures. In 2021, our sales recovered somewhat, but we believe there is still some pent-up customer demand that was not realized in 2021 due to continuing factors related to COVID-19. The sale of radiochemical products increased during the year; however, we believe the increases in revenue for 2020 and 2021 would have been greater were it not for the negative impact of COVID-19.
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To-date we have not furloughed or terminated any employees as a result of the financial impact of COVID-19. The Company has only seen a limited impact in our raw material supply chain related to the COVID-19, primarily some plastics which have been in strong demand for certain types of PPE. Alternative sources of raw materials have been obtained without any interruption to production. With the heightened concern about corporate liquidity during the COVID-19 pandemic, the Company believes that it has adequate cash to support continuing operations.
Business Strategy and Core Philosophies
Broadly defined, our business strategy is to continue to build our reputation as a leader in the cobalt, radiochemical, and nuclear medicine product industries, and to maximizing the revenue potential of our generic sodium iodine I-131 product and our expanded contract manufacturing capabilities. We also intend to continually seek ways to improve our customer service and expand our market share, with the ultimate goal of providing greater return to our shareholders. Specifically, we are continuously working with our customers to improve and develop new products to better serve the needs of the end user which, ultimately, we believe will boost product sales. A key part of our short-term and long-term business strategy is to develop and market additional generic drug products, similar to our sodium iodide I-131 product, which will offer customers high quality, reliable, and affordable products as well as increase our revenues. In addition, we will manage cash reserves and pursue additional financial support that will be structured in such a way to support further expansion of our products and services to exploit additional market opportunities.
Our core philosophy is to strive to provide high quality products and services as a profitable and environmentally conscious business, while offering excellent customer service and providing a safe and productive working environment for our employees. We operate in accordance with an ISO Quality Management System and in accordance with all current Good Manufacturing Practices under which we seek to maintain the highest level of quality and continuously improve our product manufacturing processes.
Results of Operations
Following is a summary of results of operations for 2021:
| Ÿ | Revenue in 2021 was approximately $9.6 million, which was a 3% increase compared to 2020; |
| Ÿ | Our 2021 sales in our Radiochemical Products, Cobalt Products, and Nuclear Medicine Standards business segments increased by approximately 5%, 11%, and 5% respectively as compared to 2020; |
| Ÿ | Our 2021 sales in Radiological Services and Fluorine Products business segments declined by approximately 26% and 83% respectively as compared to 2020 due to a phasing out of these business operations; |
| Ÿ | Our total gross profit rate increased to 59% in 2021 from 58% in 2020; and |
| Ÿ | Our operating costs for 2021 increased approximately 9% as compared 2020. |
| Ÿ | We had a net loss of $902,347 in 2021 compared to a net profit of $2,202,651 in 2020 |
Year Ended December 31, 2021 Compared to Year Ended December 31, 2020
The following table presents comparative revenues for the years ended December 31, 2021 and 2020:
| Revenues | For the year ended December 31, 2021 | % of Total Revenues 2021 | For the year ended December 31, 2020 | % of Total Revenues 2020 | ||||||||||||
| Radiochemical Products | $ | 4,275,044 | 44 | % | $ | 4,071,571 | 43 | % | ||||||||
| Cobalt Products | 1,354,517 | 14 | % | 1,225,580 | 13 | % | ||||||||||
| Nuclear Medicine Standards | 3,842,447 | 40 | % | 3,673,256 | 38 | % | ||||||||||
| Radiological Services | 160,159 | 2 | % | 216,139 | 2 | % | ||||||||||
| Flourine Products | 29,775 | 0 | % | 178,350 | 2 | % | ||||||||||
| Total Segments | $ | 9,661,942 | 100 | % | $ | 9,364,896 | 100 | % | ||||||||
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Revenues
Total revenues in 2021 were $9,661,942, compared to $9,364,865 in 2020, which represents an increase of $297,047, or approximately 3%. The performance of each segment is discussed in the following paragraphs.
| For the year ended | For the year ended | |||||||||||||||
| December 31, | December 31, | |||||||||||||||
| Revenues | 2021 | 2020 | $ change | % change | ||||||||||||
| Radiochemical Products | $ | 4,275,044 | $ | 4,071,571 | $ | 203,473 | 5 | % | ||||||||
| Cobalt Products | 1,354,517 | 1,225,580 | 128,937 | 11 | % | |||||||||||
| Nuclear Medicine Standards | 3,842,447 | 3,673,255 | 169,192 | 5 | % | |||||||||||
| Radiological Services | 160,159 | 216,139 | (55,980 | ) | -26 | % | ||||||||||
| Flourine Products | 29,775 | 178,350 | (148,575 | ) | -83 | % | ||||||||||
| Total Segments | 9,661,942 | 9,364,895 | 297,047 | 3 | % | |||||||||||
| Corporate revenue | — | — | — | — | ||||||||||||
| Total Consolidated | $ | 9,661,942 | $ | 9,364,895 | $ | 297,047 | 3 | % | ||||||||
Radiochemical Products
Sales of radiochemical products accounted for approximately 44% of our total sales revenue in each of 2021 and 2020. Sales in this segment increased by $203,473, or approximately 5% to $4,275,044 as compared to $4,071,571 in 2020. The increase is a result of a $354,098 or 9% increase in radiochemical product sales year over year that was primarily the result of sales of our new generic sodium iodide I-131 drug product which was launched in March 2020. We expect sales of our new product to continue to trend upward. This increase in sales was partially offset by a reduction in payments received for contract manufacturing services year over year.
In February 2020, we received approval of an ANDA to the FDA for a sodium iodide radiopharmaceutical product for use in treatment of hyperthyroidism and carcinoma of the thyroid. We began sales of this product in March 2020, and these sales have had a significant positive impact on our revenues for 2020 and 2021. We expect continued growth in sales for this product in 2022 and beyond. This is the first of several potential generic drug products we plan to submit to the FDA in the coming years. Within this segment, we also currently distribute sodium iodide (I-131) as a radiochemical product. The radiochemical product is being used for a variety of applications including industrial use and use in investigational and clinical trials. We believe that the product enhancements we have made, in addition to the generic drug products we plan to submit to the FDA, should increase future sales in this business segment.
Additionally, we have provided contract manufacturing of radiochemical products for our customers. In 2019, we entered into a manufacturing and supply agreement with a company and completed an expansion of our existing facility to support that and other contract manufacturing activities. Because of changing market conditions that company requested a termination of that contract manufacturing arrangement, and a settlement agreement was reached with that company in December 2020. As part of the settlement agreement, we received a termination payment consisting of cash and the other company’s relinquishment on all claims to expansion of our facility and all the equipment purchased by them. The settlement resulted in a significant one-time gain for us in 2020 as detailed under Other Income (Expense) below. In February 2022, we were able to sell these assets we received in the settlement agreement for another significant one-time gain. We are currently developing a business plan to produce additional radiopharmaceutical products or explore new contract manufacturing opportunities utilizing the cash from that sale.
Cobalt Products
Cobalt products sales accounted for approximately 14% of our total sales revenue in 2021 and approximately 13% in 2020. Sales in this segment increased by $128,937, or approximately 11%, in 2020 to $1,354,517, as compared to $1,225,580 in 2020. The increase in revenue within this segment was the result of increase Cobalt Sealed Source Manufacturing partially due to receipt of additional cobalt material from the ATR in 2021. Our sealed source manufacturing generates the majority of our revenue within this segment and sealed source sales depend on our ability to produce or procure this cobalt material.
In October 2014, we entered into a ten-year agreement with the DOE for the irradiation of cobalt targets. It takes many years to irradiate these cobalt targets to the desired level of activity and we anticipated having high specific activity cobalt available for our customers in 2020. However, the material had lower than expected activity and further receipt of material was delayed until about June 2021. At that point the material still had lower than expected activity, and we reached an agreement with the DOE to purchase the material at a discounted rate. Periodically we have been able to acquire recycled material that can be used to manufacture sealed sources for customers, and in some instances, our customers have supplied their own cobalt material for source fabrication. We also have access to additional low specific activity material produced by the DOE and expect to obtain, process, and sell additional cobalt products as a result during 2022.
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We have entered into cobalt supply agreements with several customers. Pursuant to these contracts, we will supply bulk cobalt-60 and, in some cases, provide source manufacturing and installation services for the customer. The terms of these cobalt contracts require some advance progress payments from each customer. The funding received under these contracts has been recorded as unearned revenue under short- and long-term liabilities in our consolidated financial statements. We recognized some of this revenue in prior years including in 2021 and 2020 when we fulfilled contract performance objectives by supplying sealed sources manufactured with cobalt from the ATR or alternate suppliers.
Nuclear Medicine Standards
Sales of nuclear medicine standards accounted for approximately 40% and 39%, of our total sales revenue in 2021 and 2020, respectively. Sales in this segment increased by $169,192, or approximately 5%, to $3,842,447 in 2021, as compared to $3,673,255 in 2020. This increase in sales is due partially to reopening of many imaging clinics and suspension of elective or non-essential imaging procedures that were closed at certain times during 2020 because of the COVID-19 pandemic. Additionally, the increase is due partially to easing of some interruption to distribution of our products due to temporary worldwide shipping restrictions the COVID-19 pandemic caused.
In 2017, affiliates of the Company purchased 75.5% of the member units of RadQual and at that time, we were named as one of the managing members of RadQual. Because of this change in member ownership and management, we have consolidated RadQual’s operations within the nuclear medicine segment for financial reporting since that time. For purposes of consolidation, all significant intercompany activity has been eliminated in the reporting process. In July 2021, we acquired the remaining 75.5% of the member units of RadQual. As a result of the acquisition, RadQual and TI Services are now our wholly-owned subsidiaries and are fully consolidated.
We anticipate that our sales of RadQual products will remain strong and that our ownership of RadQual will create significant future opportunities through new product development and expanding markets. Additionally, we will continue to work closely with TI Services using their expertise in marketing and distribution strategies to strengthen nuclear medicine product sales.
Radiological Services
Revenues from our Radiological Services segment accounted for approximately 2% of our total sales revenue in each of 2021 and 2020. Sales in this segment decreased by $55,980, or approximately 26%, from $216,139 in 2020, to $160,159 in 2021. The decrease in revenue is attributable to our termination of our contract for gemstone processing and field service activities.
Revenue from gemstone processing for the year ended December 31, 2021, was $131,650 compared to $172,555 for the same period in 2020. This was a decrease of $40,905, or approximately 24%. This decrease in revenue from gemstone processing is the result of termination of our gemstone processing activities. In January 2020, we notified our gemstone processing customer that the service contract with them was being terminated because the volume of gemstones sent for processing did not meet contract minimums. The termination activities and wrap up of this service substantially occurred in 2021 and the Company saw a steady decline in revenue from this service as production was wrapped up. In the first half of 2022, we plan to convert the spaces in the facility that had been used to perform this contract work into expanded Nuclear Medicine new product manufacturing. The loss in revenue expected from termination of the gemstone processing agreement is expected to be more than compensated for by the expansion of new nuclear medicine source products.
Revenue from field service work for the DOE had accounted for the majority of revenue in this segment. However, Radiological Field Services did not generate any Radiological Services segment sales in 2021 or 2020. This was the result the removal of this activity from our NRC license following the May 2019 contamination event. On May 2, 2019, our radiological services team was involved in a contamination event involving a breached cesium-137 source at an off-site location in the state of Washington. This work was being performed under a contract with the DOE. We have reviewed the results of the DOE investigation into this event and have implemented appropriate corrective actions. On January 5, 2021, we were notified by the DOE that we had been indemnified from any financial liability for this event under the Price Anderson Act (PAA).
Fluorine Products
In 2021, we had revenues related to Fluorine Products of $29,775 as compared to $178,350 in 2020. These revenues were related to an agreement to provide engineering and technical assistance services related to our fluorine products intellectual property. We may have additional revenue amounts in 2022 as this agreement continues. We developed our fluorine products in conjunction with the uranium de-conversion project, in order to take advantage of the anticipated need for depleted uranium de-conversion services. We established the Fluorine Products segment in 2004 to support production and sale of the gases produced using our FEP. In 2013, we made the decision to place continued formal design work on the proposed de-conversion facility on hold until such time that we are able to secure additional de-conversion services contracts. Until such time that work resumes on the project, we will limit our expenditures to essential items such as maintenance of the NRC license, land use agreements, communication with our prospective
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FEP product customers, and interface with the State of New Mexico and Lea County officials. We continue to explore opportunities for government or commercial contracting for depleted uranium deconversion services that could still utilize FEP.
During 2021, we incurred $150,196 of planning and other expenses related to the de-conversion project, as compared to $142,896 in 2020. This is an increase of $7,300, or approximately 5%, and is the result of increased professional services allocated to this project in 2021. We expect that our costs in the future will be limited to essential items such as continued interactions with our customers, the state of New Mexico, and Lea County, New Mexico.
Cost of Revenues and Gross Profit
Cost of revenues for 2021 was $3,924,142 as compared to $3,904,869 in 2020, an increase of $19,273, or less than 1%. Gross profit percentage increased to 59% for 2021, from 58% in 2020. The following table presents revenues and cost of revenues information:
For the year ended December 31, 2021 | % of Total Revenues 2021 | For the year ended December 31, 2020 | % of Total Revenues 2020 | |||||||||||||
| Total Revenues | $ | 9,661,942 | $ | 9,364,896 | 100 | % | ||||||||||
| Cost of Revenues | ||||||||||||||||
| Radiochemical Products | $ | 1,698,124 | 18 | % | $ | 1,744,442 | 19 | % | ||||||||
| Cobalt Products | 546,043 | 6 | % | 546,197 | 6 | % | ||||||||||
| Nuclear Medicine Standards | 1,679,607 | 17 | % | 1,573,730 | 17 | % | ||||||||||
| Radiological Services | 368 | 0 | % | 40,500 | 0 | % | ||||||||||
| Fluorine Products | — | — | — | — | ||||||||||||
| Total Segments | $ | 3,924,142 | 41 | % | $ | 3,904,869 | 42 | % | ||||||||
| Gross Profit | $ | 5,737,800 | $ | 5,460,027 | ||||||||||||
| Gross Profit % | 59 | % | 58 | % | ||||||||||||
During 2021, we continued to monitor and control direct costs. Raw materials used in our radiochemical products and nuclear medicine standards represented the bulk of direct costs for 2021. In each of these business segments, we have purchase agreements in place with suppliers to obtain optimum pricing. Periodically, the cost increases for these raw materials or we may also use alternate supply sources for our material which might not carry pricing as favorable as our contracted suppliers.
In 2021, we were able increase gross profit percentage in our radiochemical segment with continued growth of sales of our new generic sodium iodide I-131 drug product. In 2021, our gross profit percentage in our nuclear medicine product segment decreased due to an increase in cost of cobalt material.
Operating Costs and Expenses
Total operating costs and expenses for 2021 were $6,418,592, as compared to $5,875,700 in 2020. This is an increase of $542,892, or approximately 9%.
The following table presents operating costs and expenses for 2021 as compared to 2020:
For the year ended December 31, 2021 | For the year ended December 31, 2020 | % change | $ change | |||||||||||||
| Operating Costs and Expenses: | ||||||||||||||||
| Salaries and Contract Labor | $ | 2,687,735 | $ | 2,827,742 | -5 | % | $ | (140,007 | ) | |||||||
| General, Administrative and Consulting | 3,459,143 | 2,828,460 | 22 | % | 630,683 | |||||||||||
| Research and Development | 271,714 | 219,498 | 24 | % | 52,216 | |||||||||||
| Total operating expenses | $ | 6,418,592 | $ | 5,875,700 | 9 | % | $ | 542,892 | ||||||||
Salaries and contract labor expense decreased by $140,007, or approximately 5%, which was the result of reduced number of personnel. In addition, non-cash equity compensation expense recorded for the year ended December 31, 2021, was $86,988 as compared to $88,180 for the same period in 2020. This is a decrease of $1,192, or approximately 1%, and is the result of equity compensation recorded for outstanding stock options granted to employees and non-employees.
General administrative and consulting expenses increased to $3,459,143 in 2021, as compared to $2,828,460 in 2020, an increase of $630,683, or approximately 22%. This increase is a result of increased licenses related to our FDA approved product, increased depreciation related to the expansion of our facility, increased cost of production supplies, increased professional services expense, and increased insurance expense.
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Research and development expense was $271,714 for 2021, compared to $219,498 for 2020. This is an increase of $52,216, or approximately 24%. This increase in research and development expense was the result of increased costs associated with product development in our Nuclear Medicine business segment.
During both 2021 and 2020, we limited further investment in the planned de-conversion facility and limited further spending on the project only for expenses necessary to maintain licensing and continued interactions with New Mexico and Lea County. We will continue to delay further engineering work on the de-conversion project until we are able to secure additional contracts for de-conversion services.
Other Income (Expense)
The following table presents other income (expense) for 2021 as compared to 2020:
For the year ended December 31, 2021 | For the year ended December 31, 2020 | |||||||
| Other income (expense) | $ | 683,253 | $ | 3,637,026 | ||||
| Interest income | 111 | 3,192 | ||||||
| Interest expense | (791,532 | ) | (781,837 | ) | ||||
| Total other (expense) | $ | (108,168 | ) | $ | 2,858,381 | |||
Other income was $683,253 for 2021 as compared to other income of 3,637,026 for 2020. This is a decrease in other income of $2,953,773. The decrease is due to income recognized as part of our termination of our manufacturing and supply agreement in 2020. As part of the termination agreement, we received $500,000 cash and title to improvements and equipment that was installed in our facility. These improvements and equipment are valued at approximately $2,500,000; this was also recorded as “other income.” Additionally in 2020, we had income from PPP SBA Loans converted to grant income of $546,100 which was recorded as “other income”. In 2021 we recognized “other income” an anticipated tax refund of approximately $440,000 for the Employer Retention Credit.
Interest income in 2021 was $111 as compared to $3,192 in 2020. This decrease of $3,081 was due to decreased interest rates earned cash balances held at banks and other institutions in interest-bearing accounts.
Interest expense increased during 2021, to $791,532, from $781,837 in 2020. This is an increase of $9,695, or approximately 1%. This increased interest expense was due to an increase in interest paid for notes payable for refunds of cobalt contracts. In 2021, non-cash interest expense was $401,077 as compared to $390,938 in 2020. This is an increase of $10,139. Interest expense includes dividends accrued on our Series C Preferred Stock (as defined below) issued in 2017. In 2021, we recorded interest expense of $244,955 for dividends payable on our Series C Preferred Stock.
In connection with the 2013 Promissory Note (as defined below), we recorded $30,000 of interest expense for each of 2021 and 2020, and approximately $13,000 of non-cash interest expense related to a debt discount feature on the 2013 Promissory Note for each of 2021 and 2020.
In connection with the 2019 Promissory Note (as defined below), we recorded $40,000 and $39,000 of interest expense for 2021 and 2020 respectively, and approximately $256,000 and $249,000 of non-cash interest expense related to a debt discount feature and issuance of warrants related to the 2019 Promissory Note for 2021 and 2020 respectively.
In connection with our 2017 issuance of Series C Preferred Stock, we issued Class M Warrants and Class N Warrants. We recorded approximately $131,000 and $128,000 of non-cash interest expense for 2021 and 2020 respectively in relation to these warrants.
Net Income or Loss
Our net loss was $902,347 in 2021, compared to a net income of $2,202,651 in 2020. This is a decrease in net income of $3,104,998. Our decrease in net income was the result of $2,916,837 of other income recognized in 2020 as part of our termination agreement of our manufacturing and supply agreement and increased operating expenses in 2021 as compared to 2020.
Liquidity and Capital Resources
On December 31, 2021, we had cash and cash equivalents of $474,851 compared to $1,113,032 at December 31, 2020. Net cash used in operating activities was $161,914 in 2021, compared to net cash provided by operating activities of $1,149,625 in 2020. This represents a decrease in cash provided in operating activities of approximately $1,311,539.
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Accounts receivable at December 31, 2021 were $853,675 as compared to $796,128 at December 31, 2020. Our allowance for bad debt at December 31, 2021 was $18,910 as compared to $0 at December 31, 2020.
Inventories at December 31, 2021 were $924,775 as compared to $837,787 at December 31, 2020. A large portion of our inventory consists of Cobalt target inventory. For 2021, our target inventory accounted for approximately 48% of our work in process inventory. For 2020, our target inventory accounted for approximately 61% of our work in process inventory.
In 2020, as part of our year-end procedures, we evaluated our older target inventory held at the DOE ATR for impairment and concluded that these older design targets were fully impaired due to cumulative decay of the radioactive material. This impairment resulted in a $201,249 inventory impairment expense in 2020.
Included in our raw material inventory are raw cobalt, strontium, and other raw elements. In 2021, we determined that our raw material inventory was obsolete and fully impaired. This impairment resulted in a $33,609 inventory impairment expense in 2021.
Included in our work in process inventory are in-process and completed nuclear medicine products, irradiated cobalt and nuclear medicine-related materials and products.
We recognized a net loss of $902,347, for the year ended December 31, 2021, and have an accumulated deficit of $126,764,081 since inception. To date, our operations and plant and equipment expenditures have been funded principally from proceeds from public and private sales of debt and equity as well as through asset sales.
Net cash used in investing activities was $205,474 for 2021 and net cash provided in investing activities was $28,256 for 2020. During 2021, we used $205,474 to purchase equipment, and we used $7,744 to purchase equipment in 2020. We had proceeds from sale of equipment of $36,000 in 2020, and we had no proceeds from sale of equipment in 2021.
Financing activities used cash of $78,699 for the year ended December 31, 2021. We received proceeds from the sale of common stock in the amount of $18,890 and issued debt for proceeds of $351,255. We made principal payment on loans in the amount of $437,627 in 2021. For the year ended December 31, 2020, financing activities used cash of $637,109. We received proceeds from the sale of common stock in the amount of $16,475 and issued debt for proceeds of $871,100. In addition, we made principal payment on loans in the amount of $1,519,920 in 2020.
In February 2017, we entered into subscription agreements with certain investors, including two of our directors, for the sale of (i) an aggregate of 3,433 shares of Series C Preferred Stock, and (ii) Class M warrants to purchase an aggregate of 17,165,000 shares of our common stock (Class M Warrants), for gross proceeds of $3,433,000. The Series C Preferred Stock accrues dividends at a rate of 6% per annum, payable annually on February 17th of each year, commencing on February 17, 2018. Shares of Series C Preferred Stock are convertible at the option of the holder at any time into shares of our common stock at an initial conversion price equal to $0.10 per share, subject to adjustment. At any time after February 17, 2019, if the volume-weighted average closing price of our common stock over a period of 90 consecutive trading days is greater than $0.25 per share, we may redeem all or any portion of the outstanding Series C Preferred Stock at the original purchase price per share plus any accrued and unpaid dividends, payable in shares of common stock. All outstanding shares of Series C Preferred Stock must be redeemed by us on February 17, 2022 at the original purchase price per share, payable in cash or shares of common stock, at the option of the holder. In February 2022, based on approval of majority of the Preferred C Holders, we extended the redemption date of the Series C Preferred Stock to February 17, 2023. Holders of Series C Preferred Stock do not have any voting rights, except as required by law and in connection with certain events as set forth in the Statement of Designation of the Series C Preferred Stock. The Class M Warrants were exercisable at an exercise price of $0.12 per share, subject to adjustment as set forth in the warrant, and expired in February 2022. In February 2022, 515,000 Class M Warrants were exercised at a price of $0.12. The Company received $61,800 for the exercise.
In March 2017, we amended our 8% unsecured debentures issued that were scheduled to mature in July 2017 (the Notes) and gave the noteholders certain additional rights (the Amendment). Pursuant to the Amendment, the Notes were modified to provide each holder the right, at the holder’s option and exercisable prior to May 12, 2017, to convert all or any portion of the principal amount of the Notes, plus accrued but unpaid interest, into shares of our Series C Preferred Stock at a conversion price of $1,000 per share. Holders that elected to convert their Notes into Series C Preferred Stock received a warrant to purchase up to 3,750 shares of our common stock for each share of Series C Preferred Stock received upon conversion of the Notes, with each warrant having a five-year term, a cashless exercise feature, and an exercise price of $0.10 per share of common stock. As a result of this modification, an aggregate of $780,000 of the Notes was converted to 780 shares of Series C Preferred Stock and 2,925,000 Class N Warrants (as defined below). Residual interest was also paid to Note holders who converted of $1,515. The Notes matured in July 2017 and were repaid in full.
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As discussed above, in May 2017, we issued 780 shares of Series C Preferred Stock, and Class N warrants to purchase an aggregate of 2,925,000 shares of our common stock (Class N Warrants) upon conversion of $780,000 of the Notes. The Series C Preferred Stock accrues dividends at a rate of 6% per annum, payable annually on February 17th of each year, commencing on February 17, 2018. Shares of Series C Preferred Stock are convertible at the option of the holder at any time into shares of our common stock at an initial conversion price equal to $0.12 per share, subject to adjustment. At any time after February 17, 2019, if the volume-weighted average closing price of our common stock over a period of 90 consecutive trading days is greater than $0.25 per share, we may redeem all or any portion of the outstanding Series C Preferred Stock at the original purchase price per share plus any accrued and unpaid dividends, payable in shares of common stock. All outstanding shares of Series C Preferred Stock must be redeemed by us on February 17, 2022 at the original purchase price per share, payable in cash or shares of common stock, at the option of the holder. In February 2022, based on approval of majority of the Preferred C Holders, we extended the redemption date of the Series C Preferred Stock to February 17, 2023. Holders of Series C Preferred Stock do not have any voting rights, except as required by law and in connection with certain events as set forth in the Statement of Designation of the Series C Preferred Stock. The Class N Warrants are exercisable at an exercise price of $0.12 per share, subject to adjustment as set forth in the warrant, and have a term of five years.
In December 2013, we entered into a promissory note agreement with our then Chairman of the Board and one of our major shareholders, pursuant to which we borrowed $500,000 (the 2013 Promissory Note). The 2013 Promissory Note is secured and bears interest at 6% per annum and was originally due June 30, 2014. According to the terms of the 2013 Promissory Note, at any time, the lenders may settle any or all of the principal and accrued interest with shares of our common stock. In connection with the 2013 Promissory Note, each of the two lenders was issued 5,000,000 Class L warrants to purchase shares of our common stock at an exercise price of $0.06 per share. The warrants were immediately exercisable. In June 2014, we renegotiated the terms of the 2013 Promissory Note. Pursuant to the modification, the maturity date was extended to December 31, 2017 and each lender was granted an additional 7,500,000 Class L warrants to purchases shares of our common stock at an exercise price of $0.06 per share. The warrants were immediately exercisable. In February 2017, the 2013 Promissory Note was further modified to extend the maturity date to December 31, 2020, with all remaining terms unchanged. On December 23, 2018, all 25,000,000 Class L warrants expired. In December 2019, the 2013 Promissory Note was further modified to extend the maturity date to December 31, 2021, with all remaining terms unchanged. In January 2022, the 2013 Promissory Note was further modified to extend the maturity date to December 31, 2023, with all remaining terms unchanged.
In April 2018, we borrowed $120,000 from our Chief Executive Officer and Chairman of the Board pursuant to a promissory note (the 2018 Promissory Note). The 2018 Promissory Note accrues interest at 6% per annum, which is payable upon maturity of the 2018 Promissory Note. The 2018 Promissory Note was originally unsecured and originally matured on August 1, 2018. At any time, the holder of the 2018 Promissory Note may elect to have any or all the principal and accrued interest settled with shares of our common stock based on the average price of the shares over the previous 20 trading days. Pursuant to an amendment to the 2018 Promissory Note in June 2018, the maturity date was extended to March 31, 2019 with all other provisions remaining unchanged. Pursuant to a second amendment to the 2018 Promissory Note in February 2019, the maturity date was extended to July 31, 2019 with all other provisions remaining unchanged. Pursuant to a third amendment to the 2018 Promissory Note in July 2019, the maturity date was extended to January 31, 2020 with all other provisions remaining unchanged. Pursuant to a fourth amendment to the 2018 Promissory Note in December 2019, the maturity date was extended to December 31, 2021, the note was modified to become secured by company assets, with all other provisions remaining unchanged. In December 2021, the 2018 Promissory Note was further modified to extend the maturity date to December 31, 2023, with all remaining terms unchanged.
In December 2019, we entered into a promissory note agreement with our Chief Executive Officer, Chairman of the Board, former Chairman of the Board, and one of our major shareholders (the 2019 Promissory Note). The 2019 Promissory Note authorizes us to borrow up to $1,000,000. As of December 31, 2019, we borrowed $675,000 under the 2019 promissory note; the remaining $325,000 was borrowed in February 2020. The 2019 Promissory Note is secured and bears interest at 4% per annum and has a maturity date of December 31, 2022. According to the terms of the 2019 Promissory Note, at any time, a holder of the 2019 Promissory Note may elect to have any or all of the principal and accrued interest settled with shares of our common stock based on the average price of the shares over the previous 20 trading days. In connection with the 2019 Promissory Note, we are required to issue up to 30,000,000 Class O Warrants to purchase shares of our common stock at $0.045 per share (the Class O Warrants). The warrants are exercisable at an exercise price of $0.045 per share and have a term of five years.
In April 2021, we borrowed $250,000 from our Chief Executive Officer and Chairman of the Board pursuant to a promissory note (the April 2021 Promissory Note). The April 2021 Promissory Note bears an interest rate of 6% annually and is due December 31, 2022. At any time, the holder of the April 2021 Promissory Note may elect to have any or all of the principal and accrued interest settled with shares of our common stock based at the price of $0.11 per share. At December 31, 2021 accrued interest on the April 2021 Promissory Note totaled $10,750.
On April 23, 2020, through our wholly-owned subsidiary entered into a Loan Agreement and Promissory Note (collectively the “SBA Loan”) with KeyBank National Association pursuant to the Paycheck Protection Program (the “PPP”) under the recently enacted Coronavirus Aid, Relief, and Economic Security Act (“CARES Act”) administered by the U.S. Small Business Administration (the “SBA”). The Company received total proceeds of $546,100 from the SBA Loan.
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In July 2021, we received notification from the SBA that we received approval of forgiveness of the entire loan.
We expect that cash from operations, cash obtained through securities offerings, and our current cash balance will be sufficient to fund operations for the next twelve months. Although we may seek additional debt financing for our projects and operations in the future, there is no assurance that we will be able to secure additional debt financing on acceptable terms to us, or at all.
Goals for 2022
Based upon the investments we have made in our facilities and investments we anticipate making, and based on projects, and products developed thus far in 2022, we have the following goals for the rest of 2022:
| Ÿ | Continue to expand sales of our FDA approved sodium iodide I-131 generic drug product; |
| Ÿ | Begin development of one or more new generic drug products to further enhance revenue production within our Radiochemical segment and identify additional future generic product opportunities; |
| Ÿ | Expand sales of our nuclear medicine products and increase cash flow by offering new products and further expanding our international sales and distributor relationships; |
| Ÿ | Develop a business plan to produce additional radiopharmaceutical products or explore new contract manufacturing opportunities. |
| Ÿ | Support research and development of an advanced COVID test at a leading research hospital, with a goal of developing an accurate, inexpensive, at home saliva-based test. |
| Ÿ | Continue to expand our customer base, increase revenues, reduce production and operating costs, and attempt to achieve profitability in our core business segment operations; and |
| Ÿ | Continue to support essential tasks related to our de-conversion project and continue to pursue any opportunities to obtain additional contracts for depleted uranium de-conversion. |
Critical Accounting Estimates
Asset retirement obligation – The asset retirement obligation is based on the expected future cash flows of the decommissioning funding plan. The decommissioning funding plan is based on the estimated number of hours of specific personnel, estimated wages and disposal costs. Once the decommissioning funding plan has been developed, we use a discount rate to determine the estimated current value of the liability.
New Accounting Standards
In June 2018, the FASB issued ASU 2018-07, “Compensation-Stock Compensation (Topic 718): Improvements to Nonemployee Share-Based Payment Accounting”, which expands the scope of Topic 718 to include all share-based payment transactions for acquiring goods and services from nonemployees. ASU 2018-07 specifies that Topic 718 applies to all share-based payment transactions in which the grantor acquires goods and services to be used or consumed in its own operations by issuing share-based payment awards. ASU 2018-07 also clarifies that Topic 718 does not apply to share-based payments used to effectively provide (1) financing to the issuer or (2) awards granted in conjunction with selling goods or services to customers as part of a contract accounted for under ASC 606. The amendments in ASU 2018-07 are effective for fiscal years beginning after December 15, 2018, including interim periods within those fiscal years. We have assessed this topic and have concluded that there will be no impact of this guidance on our consolidated financial statements.
| Item 7A. | QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK |
We are a smaller reporting company, and therefore, are not required to provide the information required by this item.
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| Item 8. | FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA |
The following financial statements are included herewith and are hereby incorporated by reference:
Index to Consolidated Financial Statements
| Page No. | |
| Report of Independent Registered Public Accounting Firm | F-1 |
| Financial Statements: | |
| Consolidated Balance Sheets as of December 31, 2021 and 2020 | F-2 |
| Consolidated Statements of Operations for the years ended December 31, 2021 and 2020 | F-3 |
| Consolidated Statement of Shareholders' Equity for the years ended December 31, 2021 and 2020 | F-4 |
| Consolidated Statements of Cash Flows for the years ended December 31, 2021 and 2020 | F-5 |
| Notes to Consolidated Financial Statements | F-6 |
| Item 9. | CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE |
None.
| Item 9A. | CONTROLS AND PROCEDURES |
Evaluation of Disclosure Controls and Procedures
We maintain disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) that are designed to ensure information required to be disclosed in our reports that are filed or submitted under the Exchange Act, is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is accumulated and communicated to our management, including our principal executive and principal financial officers, or persons performing similar functions, as appropriate to allow timely decisions regarding required disclosure.
Management, with the participation of our Chief Executive Officer (CEO) and Chief Financial Officer (CFO), has conducted an evaluation (pursuant to Rule 13a-15(b) of the Exchange Act) of the effectiveness of our disclosure controls and procedures as of December 31, 2021. Based on that evaluation, our CEO and CFO concluded that our disclosure controls and procedures were effective as of December 31, 2021.
Management’s Annual Report on Internal Control over Financial Reporting
Our management is responsible for establishing and maintaining adequate internal control over financial reporting (as such term is defined in Rules 13a-15(f) and 15(d)-15(f) under the Exchange Act). Internal control over financial reporting is a process to provide reasonable assurance regarding the reliability of our financial reporting for external purposes in accordance with accounting principles generally accepted in the U.S. Internal control over financial reporting includes maintaining records that in reasonable detail accurately and fairly reflect our transactions; providing reasonable assurance that transactions are recorded as necessary for preparation of our financial statements; providing reasonable assurance that receipts and expenditures are made in accordance with management authorization; and providing reasonable assurance that unauthorized acquisition, use or disposition of company assets that could have a material effect on our financial statements would be prevented or detected on a timely basis. Because of its inherent limitations, internal control over financial reporting is not intended to provide absolute assurance that a misstatement of our financial statements would be prevented or detected.
Management conducted an evaluation of the effectiveness of our internal control over financial reporting based on the framework and criteria established in Internal Control — Integrated Framework (2013), issued by the Committee of Sponsoring Organizations of the Treadway Commission. This evaluation included review of the documentation of controls, evaluation of the design effectiveness of controls, testing of the operating effectiveness of controls and a conclusion on this evaluation. Based on this evaluation, management concluded that our internal control over financial reporting was effective as of December 31, 2021.
Changes in Internal Control over Financial Reporting
There were no changes in our internal control over financial reporting during the year ended December 31, 2021, that have materially affected, or are reasonable likely to materially affect, our internal control over financial reporting.
| 26 |
| Item 9B. | OTHER INFORMATION |
None.
| Item 9C. | DISCLOSURE REGARDING FOREIGN JURISDICTIONS THAT PREVENT INSPECTIONS |
None.
PART III.
| Item 10. | DIRECTORS, EXECUTIVE OFFICERS, AND CORPORATE GOVERNANCE |
We have adopted a Code of Ethics that applies to our principal executive officer, principal financial officer, principal accounting officer and controller, or persons performing similar functions. Our Code of Ethics is posted on our website and can be accessed, free of charge, at http://www.intisoid.com. If we waive, or implicitly waive, any material provision of the Code of Ethics that apply to our executive officers, or substantively amend the Code of Ethics, in each case that is required to be disclosed, we will disclose that fact on our website.
The other information required by this item is incorporated by reference from our definitive proxy statement for our 2022 annual meeting of shareholders, which will be filed with the SEC within 120 days after December 31, 2021.
| Item 11. | EXECUTIVE COMPENSATION |
The information required by this item is incorporated by reference from our definitive proxy statement for our 2022 annual meeting of shareholders, which will be filed with the SEC within 120 days after December 31, 2021.
| Item 12. | SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS |
The information required by this item is incorporated by reference from our definitive proxy statement for our 2022 annual meeting of shareholders, which will be filed with the SEC within 120 days after December 31, 2021.
| Item 13. | CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE |
The information required by this item is incorporated by reference from our definitive proxy statement for our 2022 annual meeting of shareholders, which will be filed with the SEC within 120 days after December 31, 2021.
| Item 14. | PRINCIPAL ACCOUNTANT FEES AND SERVICES |
The information required by this item is incorporated by reference to our definitive proxy statement for our 2022 annual meeting of shareholders, which will be filed with the SEC within 120 days after December 31, 2021.
| Item 15. | EXHIBITS, FINANCIAL STATEMENT SCHEDULES |
(a)(1) and (a)(2) Financial Statements
See the index to and the financial statements beginning on page 28, which financial statements are incorporated herein by reference.
(a)(3) Exhibits
The following documents are filed or incorporated herein by reference as exhibits to this report:
| 2.1++ | Membership Interest Purchase Agreement, dated July 8, 2021, between RadQual, LLC, International Isotopes Inc., and each of the sellers named therein (incorporated by reference to Exhibit 2.1 of the Company’s Current Report on Form 8-K filed on July 14, 2021). |
| 2.2++ | Asset Purchase Agreement, dated February 10, 2022, between International Isotopes Inc. and Pharmalogic Idaho, LLC (incorporated by reference to Exhibit 2.1 of the Company’s Current Report on Form 8-K filed on February 16, 2022). |
| 3.1 | Restated Certificate of Formation of the Company, as amended (incorporated by reference to Exhibit 3.1 of the Company’s Quarterly Report on Form 10-Q for quarter ended June 30, 2010). |
| 3.2 | Statement of Designation of the Series C Convertible Redeemable Preferred Stock of the Company (incorporated by reference to Exhibit 3.1 of the Company’s Current Report on Form 8-K filed on February 24, 2017). |
| 27 |
| 3.3 | Certificate of Amendment to Statement of Designation of the Series C Convertible Redeemable Preferred Stock International Isotopes Inc., dated February 16, 2022 (incorporated by reference to Exhibit 3.1 of the Company’s Current Report on Form 8-K filed on February 22, 2022). |
| 3.4 | Bylaws of the Company (incorporated by reference to Exhibit 3.2 of the Company's Registration Statement on Form SB-2 filed on May 1, 1997 (Registration No. 333-26269). |
| 4.1 | Form of Class N Warrant (incorporated by reference to Exhibit 4.1 of the Company’s Current Report on Form 8-K filed on May 18, 2017). |
| 10.1† | International Isotopes Inc. Amended and Restated Employee Stock Purchase Plan (incorporated by reference to Exhibit 10,1 of the Company’s Current Report on Form 8-K, filed on July 21, 2020). |
| 10.2† | International Isotopes Inc. Amended and Restated 2015 Incentive Plan (incorporated by reference to Exhibit 10.1 of the Company’s Current Report on Form 8-K, filed on July 30, 2018). |
| 10.3 | Lease Agreement (4137 Commerce Circle), dated January 20, 2020, between the Company and Adrian Rand Robison and Dorothy Robison. |
| 10.5† | Form of Director and Officer Indemnification Agreement (incorporated by reference to Exhibit 99.1 of the Company’s Current Report on Form 8-K filed on September 17, 2008). |
| 10.6 | Memorandum of Agreement, dated October 22, 2009, between the Company and the New Mexico Environment Department (incorporated by reference to Exhibit 99.1 of the Company’s Current Report on Form 8-K filed on October 27, 2009). |
| 10.7 | Gemstone Processing Agreement between the Company and Quali-Tech, Inc. (incorporated by reference to Exhibit 10.1 of Amendment No. 1 to the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2009). |
| 10.8 | Modification #1 to the Gemstone Processing Agreement, dated November 28, 2016, between the Company and QualiTech, Inc. (incorporated by reference to Exhibit 10.9 of the Company’s Annual Report on Form 10-K for the year ended December 31, 2016). |
| 10.9 | Manufacturing Agreement, dated January 30, 2006, between the Company and RadQual, LLC (incorporated by reference to Exhibit 10.2 of Amendment No. 1 to the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2009). |
| 10.10 | Registration Rights Agreement, dated October 29, 2010, among the Company and certain investors party thereto (incorporated by reference to Exhibit 99.2 of the Company’s Current Report on Form 8-K filed on November 1, 2010). |
| 10.11 | Registration Rights Agreement, dated July 27, 2012, among the Company and the purchasers named therein (incorporated by reference to Exhibit 99.4 of the Company’s Current Report on Form 8-K filed on August 2, 2012). |
| 10.12 | Registration Rights Agreement, dated February 17, 2017, among the Company and the purchasers named therein (incorporated by reference to Exhibit 10.1 of the Company’s Current Report on Form 8-K filed on February 24, 2017). |
| 10.13† | Amended and Restated Employment Agreement, dated May 16, 2012, between the Company and Stephen Laflin (incorporated by reference to Exhibit 10.2 of the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2012). |
| 10.14† | Modification #1 to the Amended and Restated Employment Agreement, dated October 12, 2016, between the Company and Stephen Laflin (incorporated by reference to Exhibit 10.15 of the Company’s Annual Report on Form 10-K for the year ended December 31, 2016). |
| 10.15 | Promissory Note Agreement, dated December 23, 2013, among the Company, Ralph Richart and John McCormack (incorporated by reference to Exhibit 10.19 of the Company’s Annual Report on Form 10-K for the year ended December 31, 2013). |
| 10.16 | Modification #1 to the Promissory Note Agreement, dated June 30, 2014, among the Company, Ralph M. Richart and John M. McCormack (incorporated by reference to Exhibit 10.1 of the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2014). |
| 28 |
| 10.17 | Modification #2 to the Promissory Note Agreement, dated February 3, 2017, among the Company, Ralph M. Richart and John M. McCormack (incorporated by reference to Exhibit 10.18 of the Company’s Annual Report on Form 10-K for the year ended December 31, 2016). |
| 10.18 | Isotope and Technical Service Order Form, dated October 2, 2014, between the Company and the U.S. Department of Energy (incorporated by reference to Exhibit 10.18 of the Company’s Annual Report on Form 10-K for the year ended December 31, 2014).** |
| 10.19 | Cobalt-60 Pellet Supply Agreement, dated April 7, 2015, between Nordion (Canada) Inc., as general partner of and on behalf of Nordion Sterilization LP, and International Isotopes Inc. (incorporated by reference to Exhibit 10.1 of the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2015).** |
| 10.20 | First Modification to Cobalt-60 Pellet Supply Agreement, effective April 21, 2017, between International Isotopes Inc. and Nordion (Canada) Inc., as general partner of and on behalf of Nordion Sterilization LP (incorporated by reference to Exhibit 10.1 of the Company’s Current Report on Form 8-K filed on May 10, 2017).** |
| 10.21 | Loan Agreement and Promissory Note, effective April 22, 2020, between International Isotopes Idaho Inc. and KeyBank National Association (incorporated by reference to Exhibit 10.1 of the Company’s Current Report on Form 8-K, filed on April 29, 2020). |
| 21.1 | Subsidiaries (incorporated by reference to Exhibit 21 of the Company’s Annual Report on Form 10-KSB for the year ended December 31, 2005). |
| 23.1+ | Consent of Haynie & Company. |
| 31.1+ | Certification of Chief Executive Officer under Section 302 of the Sarbanes-Oxley Act of 2002. |
| 31.2+ | Certification of Chief Financial Officer under Section 302 of the Sarbanes-Oxley Act of 2002. |
| 32.1* | Certification of Chief Executive Officer furnished under Section 906 of the Sarbanes-Oxley Act of 2002. |
| 32.2* | Certification of Chief Financial Officer furnished under Section 906 of the Sarbanes-Oxley Act of 2002. |
| 101.INS+ | XBRL Instance Document - the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document. |
| 101.SCH+ | XBRL Taxonomy Extension Schema Document |
| 101.CAL+ | XBRL Taxonomy Extension Calculation Linkbase Document |
| 101.DEF+ | XBRL Taxonomy Extension Definition Linkbase Document |
| 101.LAB+ | XBRL Taxonomy Extension Label Linkbase Document |
| 101.PRE+ | XBRL Taxonomy Extension Presentation Linkbase Document |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document and contained in Exhibit 101). |
| _______________________________________________ |
† This exhibit constitutes a management contract or compensatory plan or arrangement.
** Confidential treatment has been granted as to certain portions, which portions were omitted and filed separately with the Securities and Exchange Commission pursuant to a confidential treatment request.
++ Schedules have been omitted pursuant to Item 601(b)(2) of Regulation S-K. The Company hereby undertakes to supplementally furnish copies of any omitted schedules to the Securities and Exchange Commission upon request.
+ Filed herewith.
* Furnished herewith.
| Item 16. | FORM 10-K SUMMARY |
None.
| 29 |
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
| International Isotopes Inc. | |
| By: /s/ Steve T. Laflin | |
| Steve T. Laflin | |
| President, Chief Executive Officer, and Director | |
| Date: March 31, 2022 |
Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.
| March 31, 2022 | By: /s/ Steve T. Laflin |
| Steve T. Laflin | |
| President, Chief Executive Officer, and Director |
| March 31, 2022 | By: /s/ W. Matthew Cox |
| W. Matthew Cox | |
| Chief Financial Officer, Secretary |
| March 31, 2022 | By: /s/ Robert Atcher |
| Robert Atcher | |
| Director |
| March 31, 2022 | By: /s/ Christopher Grosso |
| Christopher Grosso | |
| Chairman of the Board of Directors |
| 30 |
INTERNATIONAL ISOTOPES INC. AND SUBSIDIARIES
CONSOLIDATED FINANCIAL STATEMENTS
TABLE OF CONTENTS
| Page No. | |
| Report of Independent Registered Public Accounting Firm (PCAOB ID No. |
F-1 |
| Financial Statements: | |
| Consolidated Balance Sheets as of December 31, 2021 and 2020 | F-3 |
| Consolidated Statements of Operations for the years ended December 31, 2021 and 2020 | F-4 |
| Consolidated Statement of Shareholders' Equity for the years ended December 31, 2021 and 2020 | F-5 |
| Consolidated Statements of Cash Flows for the years ended December 31, 2021 and 2020 | F-6 |
| Notes to Consolidated Financial Statements | F-7 |
| 31 |
| F-1 |
F-2
INTERNATIONAL ISOTOPES INC. AND SUBSIDIARIES
Consolidated Balance Sheets
| December 31, | December 31, | |||||||
| 2021 | 2020 | |||||||
| Assets | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | $ | ||||||
| Accounts receivable | ||||||||
| Inventories | ||||||||
| Prepaids and other current assets | ||||||||
| Total current assets | ||||||||
| Long-term assets | ||||||||
| Restricted cash | ||||||||
| Property, plant and equipment, net | ||||||||
| Capitalized lease disposal costs, net | ||||||||
| Financing lease right-of-use asset | ||||||||
| Operating lease right-of-use asset | ||||||||
| Goodwill | ||||||||
| Patents and other intangibles, net | ||||||||
| Total long-term assets | ||||||||
| Total assets | $ | $ | ||||||
| Liabilities and Stockholders' Equity | ||||||||
| Current liabilities | ||||||||
| Accounts payable | $ | $ | ||||||
| Accrued liabilities | ||||||||
| Unearned revenue | ||||||||
| Current portion of operating lease right-of-use liability | ||||||||
| Current portion of financing lease liability | ||||||||
| Current portion of related party notes payable, net of debt discount | ||||||||
| Current installments of notes payable | ||||||||
| Total current liabilities | ||||||||
| Long-term liabilities | ||||||||
| Related party notes payable, net of current portion and debt discount | ||||||||
| Notes payable, net of current portion | ||||||||
| Asset retirement obligation | ||||||||
| Financing lease liability, net of current portion | ||||||||
| Operating lease right-of-use liability, net of current portion | ||||||||
| Mandatorily redeemable convertible preferred stock, net of current portion and discount | ||||||||
| Total long-term liabilities | ||||||||
| Total liabilities | ||||||||
| Stockholders' equity | ||||||||
| Common stock, $ par value; shares authorized; and shares issued and outstanding respectively | ||||||||
| Additional paid in capital | ||||||||
| Accumulated deficit | ( | ) | ( | ) | ||||
| Equity attributable to International Isotopes Inc. stockholders | ||||||||
| Equity attributable to noncontrolling interest | ||||||||
| Total equity | ||||||||
| Total liabilities and stockholders' equity | $ | $ | ||||||
See accompanying notes to consolidated financial statements.
| F-3 |
INTERNATIONAL ISOTOPES INC. AND SUBSIDIARIES
Consolidated Statements of Operations
| Years ended December 31, | ||||||||
| 2021 | 2020 | |||||||
| Sale of product | $ | $ | ||||||
| Cost of product | ||||||||
| Gross profit | ||||||||
| Operating costs and expenses: | ||||||||
| Salaries and contract labor | ||||||||
| General, administrative and consulting | ||||||||
| Research and development | ||||||||
| Total operating expenses | ||||||||
| Operating loss | ( | ) | ( | ) | ||||
| Other income (expense): | ||||||||
| Other income (expense) | ||||||||
| Interest income | ||||||||
| Interest expense | ( | ) | ( | ) | ||||
| Total other income (expense) | ( | ) | ||||||
| Net income (loss) | ( | ) | ||||||
| Income attributable to noncontrolling interest | ||||||||
| Net income (loss) attributable to International Isotopes Inc. | $ | ( | ) | $ | ||||
| Net income per common share - basic: | $ | $ | ||||||
| Net income per common share - diluted: | $ | $ | ||||||
| Weighted average common shares outstanding - basic | ||||||||
| Weighted average common shares outstanding - diluted | ||||||||
See accompanying notes to consolidated financial statements.
| 4 |
INTERNATIONAL ISOTOPES INC AND SUBSIDIARIES
Consolidated Statement of Stockholders' Equity
Years ended December 31, 2021 and 2020
| Equity | ||||||||||||||||||||||||||||
| Attributable | Equity | |||||||||||||||||||||||||||
| to | Attributable | |||||||||||||||||||||||||||
| Additional | Internat'l | to | ||||||||||||||||||||||||||
| Common Stock | Paid-in | Accumulated | Isotopes | Noncontrolling | Total | |||||||||||||||||||||||
| Shares | Amount | Capital | Deficit | Shareholders | Interest | Equity | ||||||||||||||||||||||
| Balance December 31, 2019 | $ | $ | $ | ( | ) | $ | ( | ) | $ | $ | ( | ) | ||||||||||||||||
| Shares issued under employee stock purchase plan | ||||||||||||||||||||||||||||
| Shares issued for exercise of employee stock options | ( | ) | ||||||||||||||||||||||||||
| Stock grant | ( | ) | ||||||||||||||||||||||||||
| Stock in lieu of dividends on convertible preferred C shares | ||||||||||||||||||||||||||||
| Convertible debenture beneficial conversion feature | — | |||||||||||||||||||||||||||
| Warrants issued with convertible debentures | — | |||||||||||||||||||||||||||
| Stock based compensation | — | |||||||||||||||||||||||||||
| Net income | — | |||||||||||||||||||||||||||
| Balance December 31, 2020 | ( | ) | ||||||||||||||||||||||||||
| Shares issued under employee stock purchase plan | ||||||||||||||||||||||||||||
| Shares issued for exercise of employee stock options | ( | ) | ||||||||||||||||||||||||||
| Stock grant | ( | ) | ||||||||||||||||||||||||||
| Stock issued in lieu of dividends on preferred C shares | ||||||||||||||||||||||||||||
| Warrant exercise | ( | ) | ||||||||||||||||||||||||||
| Conversion of preferred C stock | ||||||||||||||||||||||||||||
| Conversion of preferred B stock | ||||||||||||||||||||||||||||
| Stock based compensation | — | |||||||||||||||||||||||||||
| Shares issued for purchase of 75.5% of RadQual | ( | ) | ||||||||||||||||||||||||||
| Distribution to non-controlling interest | — | ( | ) | ( | ) | |||||||||||||||||||||||
| Net (loss) income | ( | ) | ( | ) | ( | ) | ||||||||||||||||||||||
| Balance December 31, 2021 | $ | $ | $ | ( | ) | $ | $ | $ | ||||||||||||||||||||
See accompanying notes to consolidated financial statements.
| F-5 |
INTERNATIONAL ISOTOPES INC. AND SUBSIDIARIES
Consolidated Statements of Cash Flows
| Years ended December 31, | ||||||||
| 2021 | 2020 | |||||||
| Cash flows from operating activities: | ||||||||
| Net income (loss) | $ | ( | ) | $ | ||||
| Adjustments to reconcile net loss to net cash provided by (used in) operating activities: | ||||||||
| Income from contract cancelation | ( | ) | ||||||
| Depreciation and amortization | ||||||||
| (Gain)/Loss on disposal of property, plant and equipment | ( | ) | ||||||
| Bad debt expense | ||||||||
| Accretion of obligation for lease disposal costs | ||||||||
| Accretion of beneficial conversion feature | ||||||||
| Equity based compensation | ||||||||
| Forgiveness of Paycheck Protection Program Loan | ( | ) | ||||||
| Right-of-use amortization | ||||||||
| Noncash interest expense | ||||||||
| Changes in operating assets and liabilities: | ||||||||
| Accounts receivable | ( | ) | ||||||
| Prepaids and other current assets | ||||||||
| Inventories | ( | ) | ||||||
| Unearned revenues | ( | ) | ( | ) | ||||
| Accounts payable and accrued liabilities | ( | ) | ( | ) | ||||
| Net cash provided by (used in) operating activities | ( | ) | ||||||
| Cash flows from investing activities: | ||||||||
| Proceeds from sale of property, plant and equipment | ||||||||
| Purchase of property, plant, equipment and patents | ( | ) | ( | ) | ||||
| Net cash provided by (used in) investing activities | ( | ) | ||||||
| Cash flows from financing activities: | ||||||||
| Proceeds from sale of stock | ||||||||
| Proceeds from issuance of notes payable | ||||||||
| Proceeds from issuance of debt - related party | ||||||||
| Distribution to non-controlling interest | ( | ) | ||||||
| Payments on financing lease liability | ( | ) | ( | ) | ||||
| Principal payments on notes payable | ( | ) | ( | ) | ||||
| Net cash (used in) provided by financing activities | ( | ) | ( | ) | ||||
| Net change in cash and cash equivalents | ( | ) | ||||||
| Cash and cash equivalents at beginning of year | ||||||||
| Cash and cash equivalents at end of year | $ | $ | ||||||
| Supplemental disclosure of cash flow activities: | ||||||||
| Cash paid for interest | $ | $ | ||||||
| Supplemental disclosure of noncash financing and investing transactions: | ||||||||
| Decrease in accrued interest and increase in equity for conversion preferred dividends to stock | $ | $ | ||||||
| Increase in operating lease right-of-use asset and right-of-use liability for new lease | ||||||||
| Increase in equity and decrease in liability for the conversion of preferred stock | $ | $ | ||||||
| Non-cash increase of capitalized asset retirement obligation for increased funding plan | $ | $ | ||||||
| Decrease in unearned revenue and increase in notes payable for repayment plan | $ | $ | ||||||
| Increase in financing lease liability and increase in financing lease right-of-use asset for asset lease | $ | $ | ||||||
| Decrease in related party notes payable and increase in equity for amounts allocated to warrants and beneficial conversion feature | $ | $ | ||||||
| Decrease in operating lease right-of use asset and right-of-use liability for disposal of old lease | $ | $ | ||||||
| Decrease in inventory and decrease in accounts payable for cancellation of DOE contract | $ | $ | ||||||
| Increase in fixed assets for cancellation of Progenics contract | $ | $ | ||||||
| Increase in fixed assets and increase in debt for purchase of fixed asset | $ | |||||||
| Increase in equity and decrease in Non-controlling interest for acquisition of non controlling interest in RadQual and TI Services | $ | $ | ||||||
| December 31, | ||||||||
| 2021 | 2020 | |||||||
| Cash and cash equivalents | $ | $ | ||||||
| Restricted cash included in long-term assets | ||||||||
| Total cash, cash equivalents, and restricted cash shown in statement of cash flows | $ | $ | ||||||
See accompanying notes to consolidated financial statements.
| F-6 |
INTERNATIONAL ISOTOPES INC. AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
FOR THE YEARS ENDED December 31, 2021 AND 2020
NOTE 1 – DESCRIPTION OF BUSINESS AND SIGNIFICANT ACCOUNTING POLICIES
Description of business – International
Isotopes Inc. (the “Company” or “INIS”) was incorporated in Texas in November 1995. The accompanying consolidated
financial statements are presented in conformity with accounting principles generally accepted in the United States of America (“GAAP”)
and include all operations and balances of the Company and its wholly-owned subsidiaries, International Isotopes Idaho Inc., International
Isotopes Fluorine Products, Inc., and International Isotopes Transportation Services, Inc. The consolidated financial statements also
include the accounts of wholly owned subsidiaries TI Services, LLC, (“TI Services”), and RadQual, LLC (RadQual). TI Services
is headquartered in Youngstown, Ohio and was formed with RadQual in December 2010 to distribute products and services for nuclear medicine,
nuclear cardiology and Positron Emission Tomography (PET) imaging. RadQual is a global supplier of molecular imaging quality control devices,
and is now headquartered in Idaho Falls, Idaho. In addition, the Company had a
Nature of Operations – INIS and its subsidiaries, (collectively, the “Company,” “we,” “our” or “us”) manufacture a full range of nuclear medicine calibration and reference standards, a wide range of products, including cobalt teletherapy sources and a varied selection of radioisotopes and radiochemicals for medical research, pharmacy compounding, and clinical applications. The Company also distributes a varied selection of radioisotopes and radiochemicals for medical and clinical research applications. The Company also holds several patents for a fluorine extraction process that it plans to use in conjunction with a proposed commercial depleted uranium de-conversion facility which would be located in Lea County, New Mexico (the “De-Conversion Facility”). The Company’s business consists of five major business segments: Nuclear Medicine Standards, Cobalt Products, Radiochemical Products, Fluorine Products, and Radiological Services. The Company’s headquarters and all operations, with the exception of TI Services, are located in Idaho Falls, Idaho.
With the exception of certain unique products, the Company’s normal operating cycle is considered to be one year. Due to the time required to produce some cobalt products, the Company’s operating cycle for those products is considered to be two to three years. Accordingly, preliminary payments received on cobalt contracts, where shipment will not take place for greater than the operating cycle, have been recorded as unearned revenue and, depending upon estimated ship dates, classified under current or long-term liabilities on the Company’s consolidated balance sheets. These unearned revenues will be recognized as revenue in the future period during which the cobalt shipments begin. All assets expected to be realized in cash or sold during the normal operating cycle of the business are classified as current assets.
Principles of Consolidation – The consolidated financial statements include the accounts of the Company and its wholly-owned subsidiaries, including RadQual and TI Services. All significant intercompany accounts and transactions have been eliminated during consolidation.
Significant accounting policies
a) Financial instruments and cash equivalents
The carrying value of notes payable approximates
fair value because they bear interest at rates which approximate market rates. Cash and cash equivalents, totaling $
At December 31, 2021 and 2020, the Company had pledged
cash on deposit in a money market account valued at $
The Company maintains its cash accounts in various deposit accounts, the balances of which are periodically in excess of federally insured limits.
| F-7 |
b) Accounts receivable
The Company sells products mainly to recurring customers,
wherein the customer’s ability to pay has previously been evaluated. The Company generally does not require collateral. The Company
periodically reviews accounts receivable for amounts considered uncollectible and allowances are provided for uncollectible accounts when
deemed necessary. At December 31, 2021, the Company has accrued an allowance for doubtful accounts of approximately $
c) Inventories
Inventories are carried at the lower of cost or net
realizable value. Cost is determined using the first in, first out method. Work in progress inventory contains product that is undergoing
irradiation and this irradiation process can take up to three years to reach high specific activity (HSA) levels. When indicators of
inventory impairment exist, the Company measures the carrying value of the inventory against its market value, and if the carrying value
exceeds the market value, the inventory value is adjusted down accordingly. No impairment was recorded for the year ended December
31, 2021. For the year ended December 31, 2020, the Company determined $
d) Property, plant and equipment
Depreciation on property, plant and equipment is computed using the straight-line method over the estimated useful life of the asset.
Leasehold improvements are amortized over the shorter of the life of the lease or the service life of the improvements. Maintenance, repairs, and renewals that neither materially add to the value of the property nor appreciably prolong its life are charged to expense as incurred. Gains or losses on dispositions of property and equipment are included in the results of operations.
e) Goodwill and other intangibles
Goodwill is not amortized but is tested for impairment at least annually. Goodwill represents the excess of the purchase price over the fair value of net tangible and identifiable intangible assets recorded as a result of the change in ownership of RadQual. As of December 31, 2021 and 2020, there has been no impairment of goodwill.
Patents and other intangibles are amortized using the straight-line method over their estimated useful lives and are evaluated for impairment at least annually or when events or circumstances arise that indicate the existence of impairment. The Company evaluates the recoverability of identifiable intangible assets whenever events or changes in circumstances indicate that an intangible asset’s carrying amount may not be recoverable. Such circumstances could include but are not limited to: (1) a significant decrease in the market value of an asset, (2) a significant adverse change in the extent or manner in which an asset is used, or (3) an accumulation of costs significantly in excess of the amount originally expected for the acquisition of an asset. When indicators of impairment exist, the Company measures the carrying amount of the asset against the estimated undiscounted future cash flows associated with it. Should the sum of the expected future cash flows be less than the carrying value of the asset being evaluated, an impairment loss would be recognized. The impairment loss would be calculated as the amount by which the carrying value of the asset exceeds its fair value. The evaluation of asset impairment requires the Company to make assumptions about future cash flows over the life of the asset being evaluated. These assumptions require significant judgment and actual results may differ from assumed and estimated amounts. During the years ended December 31, 2021 and 2020, the Company had no impairment losses related to intangible assets.
f) Impairment of long-lived assets
Long-lived assets are reviewed for impairment annually, or when events or circumstances arise that indicate the existence of impairment, using the same evaluation process as described above for patents and other intangibles. There was no impairment recorded during the years ended December 31, 2021 and 2020.
g) Income taxes
Income taxes are accounted for under the asset and liability method. Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carry-forwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rate is recognized in income in the period that includes the enactment date.
| F-8 |
h) Use of estimates
Management of the Company has made a number of estimates and assumptions relating to the reporting of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the consolidated financial statements and reported amounts of revenues and expenses during the reporting period to prepare these consolidated financial statements in conformity with GAAP. Actual results could differ from those estimates.
i) Revenue recognition
Revenue is recognized when products are shipped. No warranty coverage or right of return provisions are provided to customers. Amounts received as prepayment on future products or services are recorded as unearned revenues and recognized as income when the product is shipped or service performed. See Note 14 Revenue Recognition.
j) Research and development costs
Research and development costs are expensed as incurred
and totaled $
The Company accounts for issuances of share-based compensation to employees in accordance with GAAP which requires the recognition of the cost of employee services received in exchange for an award of equity instruments in the financial statements and is measured based on the grant date fair value of the award. Compensation expense is recognized over the period during which an employee is required to provide service in exchange for the award (the vesting period).
For the years ended December 31, 2021 and 2020, the Company recognized share-based compensation expense of $ and $, respectively, related to stock options and stock grants. This expense is included as part of salaries and contract labor in the accompanying statements of operations.
Basic loss per share is computed on the basis of the weighted-average number of common shares outstanding during the year. Diluted loss per share is computed on the basis of the weighted-average number of common shares plus all potentially dilutive issuable common shares outstanding during the year.
| December 31, | ||||||||
| 2021 | 2020 | |||||||
| Weighted average common shares outstanding - basic | ||||||||
| Effects of dilutive shares | ||||||||
| Stock options | ||||||||
| Warrants | ||||||||
| Series B redeemable convertible preferred stock | ||||||||
| Series C redeemable convertible preferred stock | ||||||||
| Weighted average common shares outstanding - diluted | ||||||||
For the year ended December 31, 2021,
the Company had stock options outstanding,
For the year ended December 31, 2020,
the Company had stock options outstanding,
| F-9 |
The table below summarizes common stock equivalents outstanding at December 31, 2021 and 2020:
| December 31, | ||||||||
| 2021 | 2020 | |||||||
| Stock options | ||||||||
| Warrants | ||||||||
| 850 Shares of Series B redeemable convertible preferred stock | ||||||||
| 4,213 Shares of Series C redeemable convertible preferred stock | ||||||||
m) Business segments and related information
GAAP establishes standards for the way public business enterprises are to report information about operating segments in annual financial statements and requires enterprises to report selected information about operating segments in interim financial reports issued to shareholders. It also establishes standards for related disclosure about products and services, geographic areas and major customers. The Company currently operates in five business segments.
n) Recent accounting standards
In August 2020, the Financial Accounting Standards Board issued ASU 2020-06 Debt – Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging – Contracts in Entity’s Own Equity (Subtopic 815-40). The update simplifies accounting related to convertible debt instruments. The standard is effective for fiscal years beginning after December 15, 2023 including interim periods within those fiscal years. INIS is currently evaluating the effect this standard will have on its financial statements.
NOTE 2 – BUSINESS CONDITION AND LIQUIDITY
The Company has a history of recurring losses with
an accumulated deficit of $ at December 31, 2021 and net loss of $ for the year then ended. The Company’s working
capital, which includes inventory that will not be sold for up to three years, has decreased by $
On
April 5, 2019, the Company entered into a manufacturing and supply agreement with another company. The Company expanded its existing
facility and installed the equipment necessary to support this contract manufacturing opportunity. During the fourth quarter of 2020,
the contract was terminated, and the Company received cash and equipment totaling $
During the year ended December 31, 2021, the Company continued to focus on its long-standing core business segments, which consist of its radiochemical products, cobalt products, nuclear medicine standards, and radiological services segments, and in particular, the pursuit of new business opportunities within those segments.
In addition to the Company’s cobalt production agreement with the DOE, the Company entered into supply agreements in 2015 with several customers for the purchase of cobalt-60. It takes several years to irradiate cobalt targets to the desired level of activity; the shipment of cobalt-60 product to these customers is delayed until cobalt that fits the customers need can be produced. Pursuant to these cobalt-60 supply agreements, the Company will not only supply cobalt-60 to the customers but, in some instances, will also provide on-going services with respect to manufacturing and selling cobalt sources. Each contract requires quarterly progress payments to be paid by customers to the Company.
| F-10 |
Due to changes in the nuclear industry
over the past few years, the Company’s plans for the design and construction of a large-scale uranium de-conversion and fluorine
extraction facility were placed on hold. The Company expects that further activity on this project will remain on hold until the
market and industry conditions change to justify resuming design and construction of the facility. The Company will continue to
incur some costs associated with the maintenance of licenses and other necessary project investments for the proposed facility, and the
Company expects to continue to keep certain agreements in place to support resumption of project activities at the appropriate time.
The Company holds a Nuclear Regulatory Commission
(“NRC”) construction and operating license for the depleted uranium facility as well as the property agreement with Lea County,
New Mexico, where the plant is intended to be constructed. The NRC license for the de-conversion facility is a forty (40) year operating
license and is the first commercial license of this type issued in the United States. There are no other companies with a similar license
application under review by the NRC. Therefore, the NRC license represents a significant competitive barrier, and the Company believes
that it provides it with a very valuable asset. During the year ended December 31, 2021, the Company incurred costs of approximately
$
The Company expects that cash from operations and its current cash balance will be sufficient to fund operations for the next twelve months. Future liquidity and capital funding requirements will depend on numerous factors, including, contract manufacturing agreements, commercial relationships, technological developments, market factors, available credit, and voluntary warrant redemption by shareholders. There is no assurance that additional capital and financing will be available on acceptable terms to the Company or at all.
NOTE 3 – PURCHASED ASSET AND INVESTMENTS
Interest in RadQual, LLC
The Company had a
In July 2021, the Company purchased the remaining
Acquisition of Interest in TI Services, LLC
In December 2010, the Company together with RadQual,
formed a
| F-11 |
In July 2021, the Company purchased the remaining
NOTE 4 – INVENTORIES
Inventories consisted of the following for the years ended December 31, 2021 and 2020:
| 2021 | 2020 | |||||||
| Raw materials | $ | $ | ||||||
| Work in progress | ||||||||
| Finished goods | ||||||||
| Total Inventory | $ | $ | ||||||
Included in raw material inventory raw cobalt, strontium
and other raw elements. Raw material inventory is regularly reviewed for obsolescence. In 2021, the Company determined all raw material
inventory was obsolete. The remaining $
Previously, work in process included costs to irradiate
cobalt-60 material under a contract with the DOE. This material was placed in the reactor exclusively for purchase by the Company. In
2021, the company took shipment of all remaining cobalt-60 for which it had paid irradiation charges. At December 31, 2021 and 2020, the
amount of accumulated irradiation charges reported as inventory was $
NOTE 5 – PROPERTY, PLANT AND EQUIPMENT
Property, plant and equipment are summarized as follows at December 31, 2021 and 2020:
| 2021 | 2020 | Estimated Useful Lives | ||||||||
| Furniture and fixtures | $ | $ | ||||||||
| Transportation equipment | ||||||||||
| Plant and improvements | ||||||||||
| Production equipment | ||||||||||
| Accumulated depreciation | ( | ) | ( | ) | ||||||
| $ | $ | |||||||||
Included in fixed assets are assets purchased during the planning phase for the construction of a de-conversion facility in Hobbs, New Mexico. Although construction of the facility is currently on hold, the Company has determined that these assets continue to have future economic value based on what it considers a strong likelihood that construction of the facility will occur in the future.
Depreciation expense was $
NOTE 6 – PATENTS AND OTHER INTANGIBLE ASSETS
The Company owns certain patents and patents pending related to a fluorine extraction process (FEP), for various uses of some fluoride gases as fluorinating agents, and some of the RadQual nuclear medicine calibration sources. The FEP patents were developed in an effort to expand the potential markets for the high purity fluoride gases the Company will produce with its fluorine extraction process. The feasibility of expanding the fluoride gas markets through the use of this patented technology is uncertain. The RadQual product patents were developed to give RadQual a unique competitive advantage by offering calibration standards exclusive to RadQual.
In October 2012, the NRC issued the Company a 40-year construction and operating license for the de-conversion facility. Capitalized costs associated with the licensing and planning process for this license are being amortized over the 40-year life of the license.
| F-12 |
The following table summarizes the patent and intangible activity for the years ended December 31, 2021 and 2020:
| 2021 | ||||
| Beginning | $ | |||
| Additions | ||||
| Disposals | ( | ) | ||
| Ending | ||||
| Accumulated amortization | ( | ) | ||
| $ | ||||
During the year ended December 31, 2021 the Company recognized $
Patent and other intangible asset amortization is based on the remaining life of the asset and estimated amortization expense is as follows:
| Years ending December 31, | |||
| 2022 | $ | ||
| 2023 | |||
| 2024 | |||
| 2025 | |||
| 2026 | |||
| Thereafter | |||
| $ |
NOTE 7 – CONVERTIBLE DEBENTURES AND NOTES PAYABLE
Convertible debentures
As discussed in Note 9 below, in February 2017, pursuant
to a private placement transaction with certain investors, the Company issued shares of Series C Preferred Stock and warrants. In
connection with the private placement, two investors holding convertible debentures exchanged aggregate principal totaling $
Notes payable
In April 2018, the Company borrowed $
At December 31, 2021, accrued interest on the 2018
Promissory Note totaled $
In December 2013, the Company entered into a promissory
note agreement with its then Chairman of the Board and one of its major shareholders, pursuant to which the Company borrowed $
| F-13 |
At December 31, 2020, the principal balance of the
2013 Promissory Note was $
In April 2019, one of the prepaid revenue customers
requested a refund of the amounts paid. The Company entered into a note agreement to repay $
In August 2021, one of the prepaid revenue customers
requested a refund of the amounts paid. The Company entered into a note agreement to repay $
On December 20, 2019, the Company entered into a promissory note agreement with four of the Company’s major shareholders (the 2019 Promissory Note). The 2019 Promissory Note authorizes the Company to borrow up to $. As of December 31, 2019, the Company had borrowed $ under the 2019 promissory note. In February 2020, the Company borrowed an additional $. The 2019 Promissory Note bears an interest rate of % annually and is due . According to the terms of the 2019 Promissory Note, at any time, the lenders may settle any or all of the principal and accrued interest with shares of the Company’s common stock based on the average closing price of the Company’s common stock for the 20 trading days preceding the payment. In connection with the 2019 Promissory Note, the lenders were issued warrants totaling warrants to purchase shares of the Company’s common stock at $ per share (Class O Warrants). The fair value of these Class O Warrants issued totaled $ and was recorded as a debt discount and will be amortized over the life of the 2019 Promissory Note. At December 31, 2021, the remaining balance of this debt discount was $. The Company calculated a beneficial conversion feature of $ which will be accreted to interest expense over the life of the 2019 Promissory Note. At December 31, 2021, the remaining balance of this beneficial conversion feature was $. At December 31, 2021 accrued interest on the 2019 Promissory Note totaled $.
In April 2021, the Company borrowed $
At December 31, 2021, accrued interest on the 2021
Promissory Note totaled $
On April 23, 2020, the Company, through its wholly-owned
subsidiary entered into a Loan Agreement and Promissory Note (collectively the “SBA Loan”) with KeyBank National Association
pursuant to the Paycheck Protection Program (the “PPP”) under the Coronavirus Aid, Relief, and Economic Security Act (“CARES
Act”) administered by the U.S. Small Business Administration (the “SBA”). The Company received total proceeds of $
As of December 31, 2020, the Company has used the entire loan proceeds to fund qualifying expenses. As a result, the Company believed that it had met the PPP eligibility criteria for forgiveness and concluded that the loan represented, in substance, a government grant that was expected to be forgiven. As such, the Company recognized the entire loan amount as ‘Other Income’ at December 31, 2020.
In July 2021, the Company received notification from the SBA that we received approval of forgiveness of the entire loan.
| F-14 |
Notes payable as of December 31, 2021 and 2020 consist of the following:
| 2021 | 2020 | |||||||
| Note payable to related parties bearing interest at | $ | $ | ||||||
| Note payable to related parties bearing interest at | ||||||||
| Note payable to related parties net of
unamortized debt discount of $ | ||||||||
| Note payable to related parties net of unamortized debt discount of $ | ||||||||
| Note payable to customer pursuant to a refund agreement. Interest at | ||||||||
| Note payable to customer pursuant to a refund agreement. Interest at | ||||||||
| Note payable to a financial institution bearing interest at | ||||||||
| Note payable to a financial institution bearing interest at | ||||||||
| Note payable for purchase contract bearing interest at | ||||||||
| Total notes payable | ||||||||
| Less: current maturities | ( | ) | ( | ) | ||||
| Notes payable, net of current installments and debt discount | $ | $ | ||||||
Maturities of convertible debt and notes payable, excluding debt discount and debt issuance costs, at December 31, 2020, are as follows:
| Years ending December 31, | |||||
| 2022 | $ | ||||
| 2023 | |||||
| 2024 | |||||
| 2025 | |||||
| Thereafter | |||||
| $ | |||||
NOTE 8 – LEASE OBLIGATIONS
The Company leases office and warehouse space under operating leases. Right-of-use assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent its obligation to make lease payments under the lease. Operating lease, right-of-use assets, and liabilities are recognized at the lease commencement date based on the present value of lease payments over the reasonably certain lease term. The implicit rates with the Company’s operating leases are generally not determinable and the Company uses its incremental borrowing rate at the lease commencement date to determine the present value of its lease payments. The determination of the Company’s incremental borrowing rate requires judgement. The company determines its incremental borrowing rate for each lease using its then-current borrowing rate. Certain of the Company’s leases include options to extend or terminate the lease. The Company establishes the number of renewal options periods used in determining the operating lease term based upon its assessment at the inception of the operating lease. The option to renew the lease may be automatic, at the option of the Company, or mutually agreed to between the landlord and the Company. Once the facility lease term has begun, the present value of the aggregate future minimum lease payments is recorded as a right-of-use asset. Lease expense is recognized on a straight-line basis over the term of the lease.
| Year Ended | ||||||||
| December 31 | ||||||||
| 2021 | 2020 | |||||||
| Operating lease costs | $ | $ | ||||||
| Short-term operating lease costs | ||||||||
| Financing lease expense: | ||||||||
| Amortization of right-of-use assets | ||||||||
| Interest on lease liabilities | ||||||||
| Total financing lease expense | ||||||||
| Total lease expense | $ | $ | ||||||
| Right-of-use assets obtained in exchange for new operating lease liabilities | $ | $ | ||||||
| Right-of-use assets obtained in exchange for new financing lease liabilities | $ | $ | ||||||
| Weighted-average remaining lease term (years) - operating leases | ||||||||
| Weighted-average remaining lease term (years) - financing leases | ||||||||
| Weighted-average discount rate - operating leases | % | % | ||||||
| Weighted-average discount rate - financing leases | % | % | ||||||
| F-15 |
Maturities of lease liabilities as of December 31, 2021, were as follows:
| Operating leases | Finance leases | ||||
| For the years ended December 31, | |||||
| 2022 | $ | $ | |||
| 2023 | |||||
| 2024 | |||||
| 2025 | - | ||||
| 2026 | - | ||||
| Thereafter | - | ||||
| Total minimum lease obligations | |||||
| Less-amount representing interest | ( |
( | |||
| Present value of minimum lease obligations | |||||
| Current maturities | ( |
||||
| Lease obligations, net of current maturities | $ | $ | |||
NOTE 9 – SHAREHOLDERS’ EQUITY, REDEEMABLE CONVERTIBLE PREFERRED STOCK, OPTIONS AND WARRANTS
Warrants
In December 2019, the Company entered into the 2019
Promissory Note, as discussed above. In connection with the 2019 Promissory Note, the company issued Class O Warrants to purchase
shares of the Company’s common stock at a purchase price of $
In February 2020, the Company borrowed the remaining amount available for borrowings under the 2019 Promissory Note as discussed above. As a result and according to the terms of the 2019 Promissory Note, the Company issued additional Class O Warrants to purchase shares of the Company’s common stock at a purchase price of $ per share. All Class O Warrants were exercised in January 2021.
The following table summarizes warrant activity for the years ended December 31, 2021 and 2020:
| Warrants | Outstanding Shares | Weighted Average Exercise | |||||||
| Outstanding at December 31, 2019 | $ | ||||||||
| Granted | |||||||||
| Exercised | — | — | |||||||
| Forfeited | — | — | |||||||
| Outstanding at December 31, 2020 | |||||||||
| Granted | — | ||||||||
| Exercised | ( | ) | |||||||
| Forfeited | — | — | |||||||
| Outstanding at December 31, 2021 | $ | ||||||||
Warrants outstanding at December 31, 2021, included
Warrants outstanding at December 31, 2020, included
Mandatorily Redeemable Convertible Preferred Stock
The Company is authorized to issue up to shares of preferred stock, par value $ per share. The Board is authorized to set the distinguishing characteristics of each series prior to issuance, including the granting of limited or full voting rights, rights to the payment of dividends and amounts payable in event of liquidation, dissolution or winding up of the Company.
| F-16 |
At December 31, 2021, there were shares of the
Series B Convertible Redeemable Preferred Stock (the “Series B Preferred Stock”) outstanding with a mandatory redemption date
of May 2022 at $ per share, or $ in aggregate redemption value. The Series B Preferred Stock is convertible into common stock
at a conversion price of $
On February 17, 2017, the
Company entered into subscription agreements with certain investors, including two of the Company’s directors, for the sale of (i)
an aggregate of shares of Series C Preferred Stock, and (ii) Class M warrants to purchase an aggregate of
The Class M Warrants are
immediately exercisable at an exercise price of $
The
Company allocated the proceeds to the Series C Preferred Stock and Class M Warrants based on their relative fair value, which resulted
in $
On March 24, 2017, the Company
entered into an Amendment to the 8% Convertible Notes (the Amendment), pursuant to which the 8% Convertible Notes (the Notes) issued by
the Company in July 2012 were amended to give noteholders certain additional rights. Pursuant to the Amendment, the Notes were modified
to provide each holder the right, at the holder’s option and exercisable prior to May 12, 2017, to convert all or any portion of
the principal amount of the Notes, plus accrued but unpaid interest, into shares of Series C Preferred Stock at a conversion price of
$1,000 per share. Holders that elected to convert their Notes into Series C Preferred Stock received a Class N Warrant to purchase up
to 3,750 shares of the Company’s common stock for each share of Series C Preferred Stock received upon conversion of the Notes,
with each Warrant having a five-year term, a cashless exercise feature, and an exercise price of $0.10 per share of common stock. On May
12, 2017, the Company completed the retirement of $
The Class N Warrants are
immediately exercisable at an exercise price of $
The
Company allocated the proceeds to the Series C Preferred Stock and Class N Warrants based on their relative fair value, which resulted
in $
The
Company pays dividends on the Series C Preferred Stock in February each year. Dividends payable totaled $
| F-17 |
Employee Stock Purchase Plan
In September 2004, the Company’s Board approved an employee stock purchase plan for an aggregate of up to shares of the Company’s common stock. The plan allows employees to deduct up to 15% of their salary or wages each pay period to be used for the purchase of common stock at a discounted rate. The common shares will be purchased at the end of each three-month offering period or other period as determined by the Board. The plan is intended to qualify as an “employee stock purchase plan” under Section 423 of the Internal Revenue Code. An amendment and restatement of the plan was approved in July 2020 by the Company’s shareholders, which increased the number of shares available for purchase by shares. At December 31, 2021 there were shares available under the employee stock purchase plan.
During 2021 and 2020, the Company issued and shares of common stock to employees for proceeds of $ and $, respectively, in accordance with the employee stock purchase plan.
2015 Incentive Plan
In April 2015, the Company’s Board of Directors approved the International Isotopes Inc. 2015 Incentive Plan (as amended, the “2015 Plan”,) which was subsequently approved by the Company’s shareholders in July 2015. The 2015 Plan was amended and restated in July 2018 to increase the number of shares authorized for issuance under the 2015 plan by an additional shares. The 2015 Plan provides for the grant of incentive and non-qualified stock options, stock appreciation rights, restricted stock, restricted stock units, performance shares and units, and other stock or cash-based awards. The 2015 Plan amends and restates the Company’s Amended and Restated 2006 Equity Incentive Plan (the “2006 Plan”).
The 2015 Plan authorizes the issuance of up to shares of common stock, plus shares authorized, but not issued under the 2006 Plan. Unless earlier terminated, the 2015 Plan will terminate on July 13, 2025. At December 31, 2021 there were shares available for issuance under the 2015 Plan.
Non-Vested Stock Grants
Pursuant to an employment agreement with its Chief Executive Officer, the Company awarded fully vested shares of common stock to its Chief Executive Officer in February 2021 under the 2015 Plan. The number of shares awarded was based on a $ stock award using a price of $ per share. The employment agreement provides that the number of shares issued will be based on the average closing price of common stock for the 20 trading days prior to issue date but not less than $0.05 per share. Compensation expense recorded pursuant to this stock grant was $, which was determined by multiplying the number of shares awarded by the closing price of the common stock on February 28, 2021, which was $0.12 per share. The Company withheld shares of common stock to satisfy the employee’s payroll tax obligations in connection with this issuance. The net shares issued on February 28, 2021 totaled .
Pursuant to an employment agreement with its Chief Executive Officer, the Company awarded fully vested shares of common stock to its Chief Executive Officer in February 2020 under the 2015 Plan. The number of shares awarded was based on a $ stock award using a price of $ per share. The employment agreement provides that the number of shares issued will be based on the average closing price of common stock for the 20 trading days prior to issue date but not less than $0.05 per share. Compensation expense recorded pursuant to this stock grant was $, which was determined by multiplying the number of shares awarded by the closing price of the common stock on February 28, 2020, which was $0.06 per share. The Company withheld shares of common stock to satisfy the employee’s payroll tax obligations in connection with this issuance. The net shares issued on February 28, 2020 totaled .
| F-18 |
Stock Options
| Weighted | |||||||||||||||||
| Weighted | Average | ||||||||||||||||
| Average | Remaining | Average | |||||||||||||||
| Outstanding | Exercise | Contractual | Intrinsic | ||||||||||||||
| Warrants | Shares | Price | Life | Value | |||||||||||||
| Outstanding at December 31, 2019 | $ | $ | |||||||||||||||
| Granted | |||||||||||||||||
| Exercised | ( | ) | |||||||||||||||
| Forfeited | ( | ) | |||||||||||||||
| Outstanding at December 31, 2020 | |||||||||||||||||
| Granted | |||||||||||||||||
| Exercised | ( | ) | |||||||||||||||
| Forfeited | ( | ) | |||||||||||||||
| Outstanding at December 31, 2021 | |||||||||||||||||
| Exercisable at December 31, 2021 | $ | $ | |||||||||||||||
The total intrinsic value of stock options outstanding at December 31, 2021 was $. The intrinsic value for stock options outstanding is calculated as the amount by which the quoted price of $ of the Company’s common stock as of the end of 2021 exceeds the exercise price of the options.
The Company recognized $ and $ of compensation expense related to these options for the years ended December 31, 2021 and 2020, respectively. At December 31, 2021, the remaining compensation expense was $ and will be recognized over years.
In January 2021, qualified stock options were exercised under a cashless exercise. The company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect in the condensed consolidated financial statements for the year ended December 31, 2021.
In January 2021, qualified stock options were exercised under a cashless exercise. The company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect in the condensed consolidated financial statements for the year ended December 31, 2021.
In September 2021, qualified stock options were exercised under a cashless exercise. The company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect in the condensed consolidated financial statements for the year ended December 31, 2021.
In December 2021, qualified stock options were exercised under a cashless exercise. The company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect in the condensed consolidated financial statements for the year ended December 31, 2021.
In August 2020, qualified stock options were exercised under a cashless exercise. The company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect in the condensed consolidated financial statements for the year ended December 31, 2020.
During the year ended December 31, 2020, the Company granted qualified stock options to several of its employees. All options vest over a -year period with the first vesting at one-year anniversary for all grants and expiration at ten-year anniversary for all grants. The weighted average exercise price for these options was $ per share. The options have a fair value of $ as estimated on the date of issue using the Black-Scholes options pricing model with the following weighted-average assumptions: risk free interest rate of % to %, expected dividend yield rate of %, expected volatility of % to % and an expected life between and years.
| F-19 |
During the year ended December 31, 2021, the Company granted qualified stock options to several of its employees. All options vest over a -year period with the first vesting at one-year anniversary for all grants and expiration at ten-year anniversary for all grants. The weighted average exercise price for these options was $ per share. The options have a fair value of $ as estimated on the date of issue using the Black-Scholes options pricing model with the following weighted-average assumptions: risk free interest rate of % to %, expected dividend yield rate of %, expected volatility of % to % and an expected life between and years.
All options exercised were issued under a qualified plan and accordingly, there is no income tax effect in the accompanying financial statements.
NOTE 10 – INCOME TAXES
The Company paid no federal or state income taxes during 2021 and 2020. Income tax benefit on losses differed from the amounts computed by applying the recently enacted U.S. federal income tax rate of 21% to pretax losses as a result of the following:
| 2021 | 2020 | |||||||
| Income tax expense (benefit) | $ | ( | ) | $ | ||||
| Book and tax differences | ( | ) | ||||||
| State taxes net of federal benefit | ||||||||
| Change in valuation allowance | ( | ) | ||||||
| Total Income Tax Expense | $ | $ | ||||||
The tax effects of temporary differences that give rise to significant portions of the Company’s deferred tax assets (liabilities) as of December 31, 2021 and 2020 are presented below:
| 2021 | 2020 | |||||||
| Deferred income tax asset | $ | — | $ | — | ||||
| Net operating loss carryforward | ||||||||
| Valuation allowance | ( | ) | ( | ) | ||||
| Total deferred income tax asset | ||||||||
| Deferred income tax liability - depreciation | ( | ) | ( | ) | ||||
| Deferred tax asset (liability) | $ | $ | ||||||
At December 31, 2021, the Company had net operating
losses of approximately $
In accordance with GAAP, the Company has analyzed its filing positions in all jurisdictions where it is required to file income tax returns for the open tax years in such jurisdictions. The Company currently believes that all significant filing positions are highly certain and that all of its significant income tax filing positions and deductions would be sustained upon audit. Therefore, the Company has no significant reserves for uncertain tax positions, and no adjustment to such reserves was required by GAAP. No interest or penalties have been levied against the Company and none are anticipated, therefore no interest or penalty has been included in the provision for income taxes in the consolidated statements of operations.
The Internal Revenue Code contains provisions which reduce or limit the availability and utilization of net operating loss carry forwards in the event of a more than 50% change in ownership. If such an ownership change occurs with the Company, the use of these net operating losses could be limited.
NOTE 11 – COMMITMENTS AND CONTINGENCIES
Dependence on Third Parties
Sales during both 2021 to the Company’s top three customers was approximately 17% of its total gross revenue. The Company is making efforts to reduce its dependency on a small number of customers by expanding both domestic and foreign markets and through the establishment of the joint venture, TI Services to expand the distribution of products.
The production of HSA Cobalt is dependent upon the
DOE, and its prime operating contractor, which controls the reactor and laboratory operations at the ATR located outside of Idaho Falls,
Idaho.
| F-20 |
Nuclear Medicine Reference and Calibration Standard manufacturing is conducted under an exclusive contract with RadQual, which in turn has an agreement in place with several companies for distributing the products. The radiochemical product sold by the Company is supplied to the Company through agreements with several suppliers. A loss of any of these customers or suppliers could adversely affect operating results by causing a delay in production or a possible loss of sales.
Contingencies
Because all the Company’s business segments
involve the handling or use of radioactive material, the Company is required to have an operating license from the NRC and specially trained
staff to handle these materials. The Company has amended this operating license numerous times to increase the amount of material permitted
within the Company’s facility. Although this license does not currently restrict the volume of business operation performed
or projected to be performed in the upcoming year, additional processing capabilities and license amendments could be implemented that
would permit processing of other reactor-produced radioisotopes by the Company. The financial assurance required by the NRC to support
this license has been provided for with a surety bond and a restricted money market account, in the amount of $
On May 2, 2019, our radiological services team was involved in a contamination event involving a breached cesium-137 source at an off-site location in the state of Washington. This work was being performed under a contract with the DOE. We have reviewed the results of the DOE investigation into this event and have implemented appropriate corrective actions. On January 5, 2021, we were notified by the DOE that we had been indemnified from any financial liability for this event under the Price Anderson Act (PAA).
The Washington Department of Health (DOH) issued a
Notice of Violation to us in May 2020 citing two violations of our reciprocity license in the State of Washington related to the contamination
event. On December 22, 2020, the Washington DOH imposed a civil penalty of $
The U.S. Nuclear Regulatory Commission (NRC) completed an inspection of our radiological safety program and issued a Notice of Violation in June 2020 citing two different violations of our NRC materials license also related to the contamination event. The NRC notified us on October 20, 2020 that it had determined the violations were considered a Severity Level II problem. In accordance with their enforcement discretion authority the NRC has decided not to impose any civil penalty against us for these violations in recognition of our significant corrective actions. Our corrective actions included termination of all field service activities and removal of these activities from our NRC license. The NRC’s investigation of the NOV’s are now considered closed.
Defined Contribution Pension Plan
The Company has a 401(k) defined-contribution pension plan (the “401(k) Plan”). Employees are eligible to participate in the Plan after completing six months of full-time service. Participants, under provision of Internal Revenue Code § 401(k), may elect to contribute up to $19,500 of their compensation to the 401(k) Plan which includes both before-tax and Roth after-tax contribution options. Although the Company reserves the right to make discretionary matching contributions to participant accounts, there were no employer matching contributions made for either 2021 or 2020. All amounts withheld for employee contributions for 2021 were paid into the 401(k) Plan. The employer reserves the right to terminate the 401(k) Plan at any time.
NOTE 12 – ASSET RETIREMENT OBLIGATION
As part of the Company’s NRC operating license and as part of the Company’s facility lease agreements, the Company is responsible for decommissioning any facilities upon termination or relocation of operations. The Company has developed a decommissioning funding plan using guidelines provided by the NRC and has estimated the cost of decommissioning the facility in Idaho Falls. The decommissioning cost estimate is reviewed at least annually to validate the assumptions and is revised as necessary when changes in the facility processes or radiological characteristics would affect the cost of decommissioning.
| F-21 |
In accordance with GAAP, the Company has recognized future estimated decommissioning costs as an asset retirement obligation and a related capitalized lease disposal cost. The Company has recognized period-to-period changes in the liability (accretion) in the statement of operations as amortization expense. Changes resulting from revisions to the original estimate are recorded as an increase or decrease to the capitalized lease disposal cost. Capitalized lease disposal cost is amortized on a straight-line basis over the remaining life of the facility operating lease agreement.
The following summarizes the activity of the asset retirement obligation for the years ended December 31, 2021 and 2020:
|
Obligation for Lease Disposal Cost | ||
| Balance at December 31, 2019 | $ | |
| Increase in lease disposal costs | - | |
| Accretion expense/amortization expense | ||
| Balance at December 31, 2020 | ||
| Increase in lease disposal costs | ||
| Accretion expense/amortization expense | ||
| Balance at December 31, 2021 | $ | |
NOTE 13 – FAIR VALUE MEASUREMENTS
At December 31, 2021 and 2020, the Company had no assets carried at fair value.
NOTE 14 – REVENUE RECOGNITION
Revenue from Product Sales
The following tables present the Company’s revenue disaggregated by business segment and geography, based on management’s assessment of available data:
| Twelve Months Ended December 31, 2021 | Twelve Months Ended December 31, 2020 | |||||||||||||||||||||||
| U.S. | Outside U.S. | Total Revenues | % of Total Revenues | U.S. | Outside U.S. | Total Revenues | % of Total Revenues | |||||||||||||||||
| Radiochemical Products | $ | $ | $ | % | $ | $ | $ | % | ||||||||||||||||
| Cobalt Products | % | % | ||||||||||||||||||||||
| Nuclear Medicine Products | % | % | ||||||||||||||||||||||
| Radiological Services | % | % | ||||||||||||||||||||||
| Fluorine Products | % | % | ||||||||||||||||||||||
| $ | $ | $ | % | $ | $ | $ | % | |||||||||||||||||
Prior period amounts have not been adjusted under the modified retrospective approach.
Under ASC Topic 606, the Company recognizes revenue when it satisfies a performance obligation by transferring control of the promised goods or services to its customers, in an amount that reflects the consideration the Company expects to receive in exchange for the product or service.
Product sales consist of a single performance obligation that the Company satisfies at a point in time. All transactions in the radiochemical products and nuclear medicine standards segments fall into this category. Most sales transactions in the cobalt products business segment fall into this category but other cobalt product sales are recorded as deferred income as discussed below. The Company recognizes product revenue when the following events have occurred: (a) the Company has transferred physical possession of the products, (b) the Company has a present right to payment, (c) the customer has legal title to the products, and (d) the customer bears significant risks and rewards of ownership of the products. Based on the Company’s historical practices and shipping terms specified in the sales agreements and invoices, these criteria are generally met when the products are:
• Invoiced.
• Shipped from the Company’s facilities (“FOB shipping point”, which is the Company’s standard shipping term). For these sales, the Company determined that the customer is able to direct the use of, and obtain substantially all of the benefits from, the products at the time the products are shipped.
In the radiological services segment, the Company performs services under multiple types of contracts. In this segment, the Company processes gemstones and recovers various types of radioactive and/or hazardous materials from third-party facilities. Contracts for gemstone processing include two performance obligations and revenue for these contracts is recognized when each obligation is met. Recovery projects typically have only one performance obligation which is delivery of the final product or service. Under these contracts, the Company recognizes revenue once the work is complete and the customer has obtained substantially all of the benefits from the services, and the performance obligations under the contract have been met. Some recovery contracts have milestones at
| F-22 |
which point the Company can invoice and receive payments from the customer. With these contracts, the company considers each milestone a performance obligation and records revenue at the time each milestone is completed, and the customer has inspected and accepted the results of the services. The Company’s standard payment terms for its customers are generally 30 days after the Company satisfies the performance obligations.
The Company’s revenue
consists primarily of products manufactured for use in the nuclear medicine industry, distribution of radiochemicals, cobalt source manufacturing,
and providing radiological services on a contract basis for customers. With the exception of certain unique products, the Company’s
normal operating cycle is considered to be one year. Due to the time required to produce some cobalt products, the Company’s operating
cycle for those products is considered to be two to three years. Accordingly, preliminary payments
received on cobalt contracts, where shipment will not take place for greater than one year, have been recorded as unearned revenue on
the Company’s consolidated balance sheets and classified under current or long-term liabilities, depending upon estimated ship dates.
For the year ended December 31, 2021, the Company reported current unearned revenue of $
Contract Balances
The Company records a receivable
when it has an unconditional right to receive consideration after the performance obligations are satisfied. As of December 31, 2021,
and December 31, 2020, accounts receivable totaled $
Practical Expedients
The Company has elected the practical expedient not to determine whether contacts with customers contain significant financing components.
NOTE 15 – SEGMENT INFORMATION
Information related to the Company’s reportable operating business segments is shown below. The Company’s reportable segments are reported in a manner consistent with the way management evaluates the businesses. The Company identifies its reportable business segments based on differences in products and services. The accounting policies of the business segments are the same as those described in the summary of significant accounting policies.
The Company has identified the following business segments:
| Ÿ | The Nuclear Medicine Standards segment consists of the manufacture of sources and standards associated with Single Photon Emission Computed Tomography (SPECT) and Positron Emission Tomography (PET) imaging, patient positioning, and calibration or operational testing of dose measuring equipment for the nuclear pharmacy industry and includes consolidated reporting of TI Services, and the consolidated reporting of the Company’s 50/50 joint venture with RadQual. |
| Ÿ | The Cobalt Products segment includes management of a cobalt irradiation contract, fabrication of cobalt capsules for teletherapy or irradiation devices, and recycling of expended cobalt sources. |
| Ÿ | The Radiochemical Products segment includes production and distribution of Iodine-131 generic drug product and various isotopically pure radiochemicals for medical, industrial, or research applications. These products are either directly produced by the Company or are purchased in bulk from other producers and distributed by the Company in customized packages and chemical forms tailored to customer and market demands. Iodine-131 is the predominant radiochemical sold in this segment. |
| Ÿ | The Fluorine Products segment historically involved the production of small-scale qualification samples of high purity fluoride gas for various industrial applications, as well as development of laboratory and analytical processes required to support the planned uranium de-conversion and fluorine extraction facility. During 2013, these testing activities were completed, and the pilot plant facility was closed. The Company has developed or acquired all patent rights to these processes. Future work in this segment will involve license support and, as financing permits, further work related to the de-conversion facility. |
| Ÿ | The Radiological Services segment concerns a wide array of miscellaneous services that consists of gemstone processing and source disposal. |
The following presents certain segment information as of and for the years ended December 31, 2021 and 2020:
| F-23 |
| Sale of product | 2021 | 2020 | ||||
| Radiochemical products | $ | $ | ||||
| Cobalt products | ||||||
| Nuclear medicine standards | ||||||
| Radiological services | ||||||
| Fluorine products | ||||||
| Total segments | ||||||
| Corporate revenue | - | - | ||||
| Total consolidated | $ | $ | ||||
| Depreciation and amortization | 2021 | 2020 | ||||
| Radiochemical products | $ | $ | ||||
| Cobalt products | ||||||
| Nuclear medicine standards | ||||||
| Radiological services | ||||||
| Fluorine products | ||||||
| Total segments | ||||||
| Corporate depreciation and amortization | ||||||
| Total consolidated | $ | $ | ||||
| Segment income (loss) | 2021 | 2020 | ||||
| Radiochemical products | $ | $ | ||||
| Cobalt products | ||||||
| Nuclear medicine standards | ||||||
| Radiological services | ||||||
| Fluorine products | ( |
|||||
| Total segments | ||||||
| Corporate loss | ( |
( | ||||
| Total consolidated | $ | ( |
$ | |||
| Expenditures for segment assets | 2021 | 2020 | ||||
| Radiochemical products | $ | $ | ||||
| Cobalt products | - | |||||
| Nuclear medicine standards | - | |||||
| Radiological services | - | - | ||||
| Fluorine products | ||||||
| Total segments | ||||||
| Corporate purchases | - | |||||
| Total consolidated | $ | $ | ||||
| Segment assets | 2021 | 2020 | ||||
| Radiochemical products | $ | $ | ||||
| Cobalt products | ||||||
| Nuclear medicine standards | ||||||
| Radiological services | ||||||
| Fluorine products | ||||||
| Total segments | ||||||
| Corporate assets | ||||||
| Total consolidated | $ | $ | ||||
NOTE 16 – SUBSEQUENT EVENTS
In March 2022, qualified stock options were exercised under a cashless exercise. The Company withheld shares to satisfy the exercise price and issued shares of common stock. The options exercised were granted under the 2015 Plan, and, accordingly, there was not any income tax effect.
In February 2022, Class M Warrants were exercised at a price of
$
On February 10, 2022, the Company entered into an Asset Purchase Agreement
with Pharmalogic Idaho, LLC (“Pharmalogic”), pursuant to which the Company agreed to sell certain assets to Pharmalogic for
$
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On February 16, 2022, the Company received approval of a modification to the term of its Series C Convertible Redeemable Preferred Stock from a majority of the outstanding shares of the Series C Preferred Stock. The modification extends the maturity date of the Series C Preferred for approximately one year to February 28, 2023. All other terms in the Series C Preferred Stock remain unchanged.
On March 31, 2022, the Company paid in full the April
2021 Promissory Note. This note originated in April 2021 as the Company borrowed $250,000 from its Chief
Executive Officer and Chairman of the Board pursuant to a promissory note. The March 2022 pay off included $
F-24