§ 32.1 - Purpose and scope.

§ 32.2 - Definitions.

§ 32.3 - Maintenance of records.

§ 32.8 - Information collection requirements: OMB approval.

Subpart A - Exempt Concentrations and Items

§ 32.11 - Introduction of byproduct material in exempt concentrations into products or materials, and transfer of ownership or possession: Requirements for license.

§ 32.12 - Same: Records and material transfer reports.

§ 32.13 - Same: Prohibition of introduction.

§ 32.14 - Certain items containing byproduct material; requirements for license to apply or initially transfer.

§ 32.15 - Same: Quality assurance, prohibition of transfer, and labeling.

§ 32.16 - Certain items containing byproduct material: Records and reports of transfer.

§ 32.17 - Resins containing scandium-46 and designed for sand-consolidation in oil wells: Requirements for license to manufacture, or initially transfer for sale or distribution.

§ 32.18 - Manufacture, distribution and transfer of exempt quantities of byproduct material: Requirements for license.

§ 32.19 - Same: Conditions of licenses.

§ 32.20 - Same: Records and material transfer reports.

§ 32.21 - Radioactive drug: Manufacture, preparation, or transfer for commercial distribution of capsules containing carbon-14 urea each for “in vivo” diagnostic use for humans to persons exempt from licensing; Requirements for a license.

§ 32.22 - Self-luminous products containing tritium, krypton-85 or promethium-147: Requirements for license to manufacture, process, produce, or initially transfer.

§ 32.23 - Same: Safety criteria.

§ 32.24 - Same: Table of organ doses.

§ 32.25 - Conditions of licenses issued under § 32.22: Quality control, labeling, and reports of transfer.

§ 32.26 - Gas and aerosol detectors containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer.

§ 32.27 - Same: Safety criteria.

§ 32.28 - Same: Table of organ doses.

§ 32.29 - Conditions of licenses issued under § 32.26: Quality control, labeling, and reports of transfer.

§ 32.30 - Certain industrial devices containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer.

§ 32.31 - Certain industrial devices containing byproduct material: Safety criteria.

§ 32.32 - Conditions of licenses issued under § 32.30: Quality control, labeling, and reports of transfer.

§ 32.40 - Schedule A—Prototype tests for automobile lock illuminators.

§ 32.21a - Same: Conditions of license.

Subpart B - Generally Licensed Items

§ 32.51 - Byproduct material contained in devices for use under § 31.5; requirements for license to manufacture, or initially transfer.

§ 32.52 - Same: material transfer reports and records.

§ 32.53 - Luminous safety devices for use in aircraft: Requirements for license to manufacture, assemble, repair or initially transfer.

§ 32.54 - Same: Labeling of devices.

§ 32.55 - Same: Quality assurance, prohibition of transfer.

§ 32.56 - Same: Material transfer reports.

§ 32.57 - Calibration or reference sources containing americium-241 or radium-226: Requirements for license to manufacture or initially transfer.

§ 32.58 - Same: Labeling of devices.

§ 32.59 - Same: Leak testing of each source.

§ 32.60 - [Reserved]

§ 32.61 - Ice detection devices containing strontium-90; requirements for license to manufacture or initially transfer.

§ 32.62 - Same: Quality assurance; prohibition of transfer.

§ 32.71 - Manufacture and distribution of byproduct material for certain in vitro clinical or laboratory testing under general license.

§ 32.101 - Schedule B—prototype tests for luminous safety devices for use in aircraft.

§ 32.102 - Schedule C—prototype tests for calibration or reference sources containing americium-241 or radium-226.

§ 32.103 - Schedule D—prototype tests for ice detection devices containing strontium-90.

§ 32.51a - Same: Conditions of licenses.

Subpart C - Specifically Licensed Items

§ 32.72 - Manufacture, preparation, or transfer for commercial distribution of radioactive drugs containing byproduct material for medical use under part 35.

§ 32.74 - Manufacture and distribution of sources or devices containing byproduct material for medical use.

§ 32.110 - Acceptance sampling procedures under certain specific licenses.

§ 32.201 - Serialization of nationally tracked sources.

Subpart D - Sealed Source and Device Registration

§ 32.210 - Registration of product information.

§ 32.211 - Inactivation of certificates of registration of sealed sources and devices.

Subpart E - Violations

§ 32.301 - Violations.

§ 32.303 - Criminal penalties.