1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter C - DRUGS: GENERAL
  5. Part 212 - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
  6. 21 CFR Subpart K
21 CFR Subpart K
Complaint Handling
June 25, 2020
§
212.100
What do I do if I receive a complaint about a PET drug product produced at my facility?
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Subpart J Distribution
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Subpart L Records

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