FDA Inspection 1299382 — American Supplement Manufacturing Corporation
The FDA completed an inspection of American Supplement Manufacturing Corporation on January 21, 2026 in Buena Park, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 7 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- January 21, 2026
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Buena Park, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15425 | 21 CFR 111.15(i) | Hand-washing facilities |
| 15433 | 21 CFR 111.15(d)(1) | Animals and pests in facility |
| 15496 | 21 CFR 111.27(b) | Instruments - calibration |
| 15953 | 21 CFR 111.113(a)(1) | Quality control production, process control; material review, disposition |
| 22843 | 21 CFR 111.70(b) | Specifications - components |
| 22847 | 21 CFR 111.70(e) | Specifications - finished dietary supplement |
| 22890 | 21 CFR 111.260 | Batch record - required information |