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title 21
Food and Drugs
chapter I-i3
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
part 212
PART 212—CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
subpart K
Subpart K—Complaint Handling
Subpart K. Subpart K—Complaint Handling
§ 212.100 - What do I do if I receive a complaint about a PET drug product produced at my facility?
