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title 21
Food and Drugs
chapter I-i1
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) (Parts 100 to 169)
part 111
PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
subpart P
Subpart P—Records and Recordkeeping
Subpart P. Subpart P—Records and Recordkeeping
§ 111.605 - What requirements apply to the records that you make and keep?
§ 111.610 - What records must be made available to FDA?
