FDA Inspection 662603 — Desert Rose Manufacturing, Inc
The FDA completed an inspection of Desert Rose Manufacturing, Inc on May 14, 2010 in Anthony, NM. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 13 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 14, 2010
- Fiscal Year
- 2010
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Anthony, NM (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15410 | 21 CFR 111.14(b)(2) | Personnel - records - training |
| 15425 | 21 CFR 111.15(i) | Hand-washing facilities |
| 15429 | 21 CFR 111.15(k) | Sanitation supervisors - assigned |
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15586 | 21 CFR 111.155(e) | Components - contamination, deterioration, mix-ups |
| 15675 | 21 CFR 111.315(b) | Sampling plans; establish, follow |
| 15723 | 21 CFR 111.365(i) | Metal, foreign material |
| 15761 | 21 CFR 111.205(b)(1) | Master manufacturing record - specifications; quality |
| 15828 | 21 CFR 111.70(a) | Specifications - manufacturing process |
| 15862 | 21 CFR 111.75(a)(2) | Appropriate tests, examinations; certificate of analysis |
| 15882 | 21 CFR 111.75(h) | Tests, examinations - scientifically valid |
| 15893 | 21 CFR 111.80(c) | Specifications - representative samples; finished batch |
| 15944 | 21 CFR 111.105(i) | QC - required operations master manufacturing/batch records |