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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter J - Radiological Health |
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Part 1002 - Records and Reports |
| Subpart A - General Provisions |
| § 1002.1 - Applicability. |
| § 1002.2 - [Reserved] |
| § 1002.3 - Notification to user of performance and technical data. |
| § 1002.4 - Confidentiality of information. |
| § 1002.7 - Submission of data and reports. |
| Subpart B - Required Manufacturers' Reports for Listed Electronic Products |
| § 1002.10 - Product reports. |
| § 1002.11 - Supplemental reports. |
| § 1002.12 - Abbreviated reports. |
| § 1002.13 - Annual reports. |
| Subpart C - Manufacturers' Reports on Accidental Radiation Occurrences |
| § 1002.20 - Reporting of accidental radiation occurrences. |
| Subpart D - Manufacturers' Records |
| § 1002.30 - Records to be maintained by manufacturers. |
| § 1002.31 - Preservation and inspection of records. |
| Subpart E - Dealer and Distributor Records |
| § 1002.40 - Records to be obtained by dealers and distributors. |
| § 1002.41 - Disposition of records obtained by dealers and distributors. |
| § 1002.42 - Confidentiality of records furnished by dealers and distributors. |
| Subpart F - Exemptions From Records and Reports Requirements |
| § 1002.50 - Special exemptions. |
| § 1002.51 - Exemptions for manufacturers of products intended for the U.S. Government. |