CFR section
21 CFR 111.525(a): What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?
PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS · Subpart N-Returned Dietary Supplements
Key facts
| Citation | 21 CFR 111.525(a) |
|---|---|
| Section | What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing? |
| Part | PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS |
| Subpart | Subpart N-Returned Dietary Supplements |
| Subchapter | 21 CFR B Food |
| Product types cited | Food/Cosmetics |
| Regulation text (excerpt) | (a) You must ensure that any returned dietary supplements that are reprocessed meet all product specifications established in accordance with § 111.70(e); and |
At a glance
- 1–9 Inspections citing this section
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.