FDA Inspection 1204344 — Quality Supplement Manufacturing, Inc.
The FDA completed an inspection of Quality Supplement Manufacturing, Inc. on May 4, 2023 in Oklahoma City, OK. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 9 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 4, 2023
- Fiscal Year
- 2023
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Oklahoma City, OK (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15404 | 21 CFR 111.12(c) | Personnel - education, training, experience |
| 15533 | 21 CFR 111.255(c) | Batch record - follow master |
| 15550 | 21 CFR 111.260(j) | Batch record - manufacture |
| 15569 | 21 CFR 111.260(n) | Batch record - reprocessing |
| 15744 | 21 CFR 111.210(h)(2) | Master manufacturing record - sampling, tests, examinations |
| 15839 | 21 CFR 111.70(e) | Specifications - identity, purity, strength, composition |
| 15882 | 21 CFR 111.75(h) | Tests, examinations - scientifically valid |
| 15885 | 21 CFR 111.77(a) | Specifications not met - reject, quality control |
| 16022 | 21 CFR 111.140(b)(3)(iv) | Material review, disposition, follow-up; identification |