| 10:1.0.1.1.22.0.91.1 | SECTION 32.1
| 32.1 Purpose and scope. | |
| 10:1.0.1.1.22.0.91.2 | SECTION 32.2
| 32.2 Definitions. | |
| 10:1.0.1.1.22.0.91.3 | SECTION 32.3
| 32.3 Maintenance of records. | |
| 10:1.0.1.1.22.0.91.4 | SECTION 32.8
| 32.8 Information collection requirements: OMB approval. | |
| 10:1.0.1.1.22.1 | SUBPART A
| Subpart A - Exempt Concentrations and Items | |
| 10:1.0.1.1.22.1.91.1 | SECTION 32.11
| 32.11 Introduction of byproduct material in exempt concentrations into products or materials, and transfer of ownership or possession: Requirements for license. | |
| 10:1.0.1.1.22.1.91.2 | SECTION 32.12
| 32.12 Same: Records and material transfer reports. | |
| 10:1.0.1.1.22.1.91.3 | SECTION 32.13
| 32.13 Same: Prohibition of introduction. | |
| 10:1.0.1.1.22.1.91.4 | SECTION 32.14
| 32.14 Certain items containing byproduct material; requirements for license to apply or initially transfer. | |
| 10:1.0.1.1.22.1.91.5 | SECTION 32.15
| 32.15 Same: Quality assurance, prohibition of transfer, and labeling. | |
| 10:1.0.1.1.22.1.91.6 | SECTION 32.16
| 32.16 Certain items containing byproduct material: Records and reports of transfer. | |
| 10:1.0.1.1.22.1.91.7 | SECTION 32.18
| 32.18 Manufacture, distribution and transfer of exempt quantities of byproduct material: Requirements for license. | |
| 10:1.0.1.1.22.1.91.8 | SECTION 32.19
| 32.19 Same: Conditions of licenses. | |
| 10:1.0.1.1.22.1.91.9 | SECTION 32.20
| 32.20 Same: Records and material transfer reports. | |
| 10:1.0.1.1.22.1.91.10 | SECTION 32.21
| 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. | |
| 10:1.0.1.1.22.1.91.11 | SECTION 32.21a
| 32.21a Same: Conditions of license. | |
| 10:1.0.1.1.22.1.91.12 | SECTION 32.22
| 32.22 Self-luminous products containing tritium, krypton-85 or promethium-147: Requirements for license to manufacture, process, produce, or initially transfer. | |
| 10:1.0.1.1.22.1.91.13 | SECTION 32.23
| 32.23 Same: Safety criteria. | |
| 10:1.0.1.1.22.1.91.14 | SECTION 32.24
| 32.24 Same: Table of organ doses. | |
| 10:1.0.1.1.22.1.91.15 | SECTION 32.25
| 32.25 Conditions of licenses issued under § 32.22: Quality control, labeling, and reports of transfer. | |
| 10:1.0.1.1.22.1.91.16 | SECTION 32.26
| 32.26 Gas and aerosol detectors containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer. | |
| 10:1.0.1.1.22.1.91.17 | SECTION 32.27
| 32.27 Same: Safety criteria. | |
| 10:1.0.1.1.22.1.91.18 | SECTION 32.28
| 32.28 Same: Table of organ doses. | |
| 10:1.0.1.1.22.1.91.19 | SECTION 32.29
| 32.29 Conditions of licenses issued under § 32.26: Quality control, labeling, and reports of transfer. | |
| 10:1.0.1.1.22.1.91.20 | SECTION 32.30
| 32.30 Certain industrial devices containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer. | |
| 10:1.0.1.1.22.1.91.21 | SECTION 32.31
| 32.31 Certain industrial devices containing byproduct material: Safety criteria. | |
| 10:1.0.1.1.22.1.91.22 | SECTION 32.32
| 32.32 Conditions of licenses issued under § 32.30: Quality control, labeling, and reports of transfer. | |
| 10:1.0.1.1.22.2 | SUBPART B
| Subpart B - Generally Licensed Items | |
| 10:1.0.1.1.22.2.91.1 | SECTION 32.51
| 32.51 Byproduct material contained in devices for use under § 31.5; requirements for license to manufacture, or initially transfer. | |
| 10:1.0.1.1.22.2.91.2 | SECTION 32.51a
| 32.51a Same: Conditions of licenses. | |
| 10:1.0.1.1.22.2.91.3 | SECTION 32.52
| 32.52 Same: material transfer reports and records. | |
| 10:1.0.1.1.22.2.91.4 | SECTION 32.53
| 32.53 Luminous safety devices for use in aircraft: Requirements for license to manufacture, assemble, repair or initially transfer. | |
| 10:1.0.1.1.22.2.91.5 | SECTION 32.54
| 32.54 Same: Labeling of devices. | |
| 10:1.0.1.1.22.2.91.6 | SECTION 32.55
| 32.55 Same: Quality assurance, prohibition of transfer. | |
| 10:1.0.1.1.22.2.91.7 | SECTION 32.56
| 32.56 Same: Material transfer reports. | |
| 10:1.0.1.1.22.2.91.8 | SECTION 32.57
| 32.57 Calibration or reference sources containing americium-241 or radium-226: Requirements for license to manufacture or initially transfer. | |
| 10:1.0.1.1.22.2.91.9 | SECTION 32.58
| 32.58 Same: Labeling of devices. | |
| 10:1.0.1.1.22.2.91.10 | SECTION 32.59
| 32.59 Same: Leak testing of each source. | |
| 10:1.0.1.1.22.2.91.11 | SECTION 32.60
| 32.60 [Reserved] | |
| 10:1.0.1.1.22.2.91.12 | SECTION 32.61
| 32.61 Ice detection devices containing strontium-90; requirements for license to manufacture or initially transfer. | |
| 10:1.0.1.1.22.2.91.13 | SECTION 32.62
| 32.62 Same: Quality assurance; prohibition of transfer. | |
| 10:1.0.1.1.22.2.91.14 | SECTION 32.71
| 32.71 Manufacture and distribution of byproduct material for certain in vitro clinical or laboratory testing under general license. | |
| 10:1.0.1.1.22.3 | SUBPART C
| Subpart C - Specifically Licensed Items | |
| 10:1.0.1.1.22.3.91.1 | SECTION 32.72
| 32.72 Manufacture, preparation, or transfer for commercial distribution of radioactive drugs containing byproduct material for medical use under part 35. | |
| 10:1.0.1.1.22.3.91.2 | SECTION 32.74
| 32.74 Manufacture and distribution of sources or devices containing byproduct material for medical use. | |
| 10:1.0.1.1.22.3.91.3 | SECTION 32.201
| 32.201 Serialization of nationally tracked sources. | |
| 10:1.0.1.1.22.4 | SUBPART D
| Subpart D - Sealed Source and Device Registration | |
| 10:1.0.1.1.22.4.91.1 | SECTION 32.210
| 32.210 Registration of product information. | |
| 10:1.0.1.1.22.4.91.2 | SECTION 32.211
| 32.211 Inactivation of certificates of registration of sealed sources and devices. | |
| 10:1.0.1.1.22.5 | SUBPART E
| Subpart E - Violations | |
| 10:1.0.1.1.22.5.91.1 | SECTION 32.301
| 32.301 Violations. | |
| 10:1.0.1.1.22.5.91.2 | SECTION 32.303
| 32.303 Criminal penalties. | |