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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 H - Medical Devices |
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Part 820 - Quality System Regulation |
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Subpart M - Records |
| § 820.180 - General requirements. |
| § 820.181 - Device master record. |
| § 820.184 - Device history record. |
| § 820.186 - Quality system record. |
| § 820.198 - Complaint files. |