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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 O
Subpart O—Product Complaints
Subpart O. Subpart O—Product Complaints
§ 111.553 - What are the requirements under this subpart O for written procedures?
§ 111.560 - What requirements apply to the review and investigation of a product complaint?
§ 111.570 - Under this subpart O, what records must you make and keep?
