FDA Inspection 1301858 — Auri Nutra, Inc.
The FDA completed an inspection of Auri Nutra, Inc. on February 4, 2026 in Farmingdale, NY. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 12 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- February 4, 2026
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Farmingdale, NY (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15702 | 21 CFR 111.320(b) | Examination, testing; scientifically valid |
| 15723 | 21 CFR 111.365(i) | Metal, foreign material |
| 15858 | 21 CFR 111.75(a)(1)(i) | Component - verify identity, dietary ingredient |
| 15953 | 21 CFR 111.113(a)(1) | Quality control production, process control; material review, disposition |
| 15983 | 21 CFR 111.123(a)(7) | Quality control operations - finished batch, specifications |
| 15986 | 21 CFR 111.123(b)(2) | Quality control - batch, product specifications |
| 22843 | 21 CFR 111.70(b) | Specifications - components |
| 22847 | 21 CFR 111.70(e) | Specifications - finished dietary supplement |
| 22855 | 21 CFR 111.90(b)(1) | Reprocessed, dietary supplement - no material review |
| 22888 | 21 CFR 111.210 | Master manufacturing record - record requirements |
| 22890 | 21 CFR 111.260 | Batch record - required information |
| 22911 | 21 CFR 111.535(b) | Make and keep records - returned dietary supplements |