SUBPART N—Returned Dietary Supplements (§111.503 to §111.535) - Title 21 - Food and Drugs CFR - USA Laws Searching

CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION (parts 100 to 191) > PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS > SUBPART N—Returned Dietary Supplements (§111.503 to §111.535)

SUBPART N—Returned Dietary Supplements (§111.503 to §111.535)

111.503—What are the requirements under this subpart N for written procedures?
111.510—What requirements apply when a returned dietary supplement is received?
111.515—When must a returned dietary supplement be destroyed, or otherwise suitably disposed of?
111.520—When may a returned dietary supplement be salvaged?
111.525—What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?
111.530—When must an investigation be conducted of your manufacturing processes and other batches?
111.535—Under this subpart N, what records must you make and keep?