FDA Inspection 929821 — GRQ Consulting Inc. dba Trifecta
The FDA completed an inspection of GRQ Consulting Inc. dba Trifecta on June 17, 2015 in Reno, NV. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 9 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 17, 2015
- Fiscal Year
- 2015
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Reno, NV (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15543 | 21 CFR 111.260(c) | Batch record - date, time; maintenance |
| 15548 | 21 CFR 111.260(h) | Batch record - results; testing, examination; batch |
| 15582 | 21 CFR 111.155(e) | Components - contamination, deterioration, mix-ups |
| 15646 | 21 CFR 111.460(a) | Hold, identify - in-process material |
| 15721 | 21 CFR 111.365(k) | Processing lines, major equipment - contents |
| 15725 | 21 CFR 111.365(g) | Identifying, holding - contamination, mix-ups |
| 15737 | 21 CFR 111.210(h)(5) | Corrective action plans |
| 15744 | 21 CFR 111.210(h)(2) | Master manufacturing record - sampling, tests, examinations |