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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 111 — CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart O — Product Complaints
Federal (United States) · Regulations
Subpart O — Product Complaints
3 sections
3 sections
21 C.F.R. § 111.553
What are the requirements under this subpart O for written procedures?
21 C.F.R. § 111.560
What requirements apply to the review and investigation of a product complaint?
21 C.F.R. § 111.570
Under this subpart O, what records must you make and keep?
Subpart O — Product Complaints | Federal (United States) Regulations | Justis AI