1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter H - MEDICAL DEVICES
  5. Part 803 - MEDICAL DEVICE REPORTING
  6. 21 CFR Subpart C
21 CFR Subpart C
User Facility Reporting Requirements
June 25, 2020
§
803.30
If I am a user facility, what reporting requirements apply to me?
§
803.32
If I am a user facility, what information must I submit in my individual adverse event reports?
§
803.33
If I am a user facility, what must I include when I submit an annual report?
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Subpart B Generally Applicable Requirements for Individual Adverse Event Reports
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Subpart D Importer Reporting Requirements

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