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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 D
Subpart D—Facilities and Equipment
Subpart D. Subpart D—Facilities and Equipment
§ 212.30 - What requirements must my facilities and equipment meet?
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