FDA Inspection 1300052 — Purever Nutrition Inc
The FDA completed an inspection of Purever Nutrition Inc on Nov 18, 2025 in Richmond. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 7 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 18, 2025
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Richmond (Canada)
Citations
| ID | CFR | Description |
|---|---|---|
| 15953 | 21 CFR 111.113(a)(1) | Quality control production, process control; material review, disposition |
| 16048 | 21 CFR 111.515 | Returned dietary supplement - destroyed |
| 22823 | 21 CFR 111.15(b) | Physical plant - clean and sanitary |
| 22843 | 21 CFR 111.70(b) | Specifications - components |
| 22847 | 21 CFR 111.70(e) | Specifications - finished dietary supplement |
| 22888 | 21 CFR 111.210 | Master manufacturing record - record requirements |
| 22890 | 21 CFR 111.260 | Batch record - required information |