Records

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Medical Devices
  6. Quality System Regulation
  7. Records

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Section
820.180

General requirements.

Section
820.181

Device master record.

Section
820.184

Device history record.

Section
820.186

Quality system record.

Section
820.198

Complaint files.