FDA Inspection 846211 — Liquid Manufacturing, L.L.C.
The FDA completed an inspection of Liquid Manufacturing, L.L.C. on September 6, 2013 in Brighton, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 10 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 6, 2013
- Fiscal Year
- 2013
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Brighton, MI (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15496 | 21 CFR 111.27(b) | Instruments - calibration |
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15671 | 21 CFR 111.315 | Laboratory control processes - requirements |
| 15702 | 21 CFR 111.320(b) | Examination, testing; scientifically valid |
| 15740 | 21 CFR 111.210(h)(3)(ii)(A) | Instructions; components; weight, measure |
| 15748 | 21 CFR 111.210(f) | Master manufacturing record theoretical and expected yield |
| 15831 | 21 CFR 111.70(b)(3) | Specifications - contamination limits |
| 15858 | 21 CFR 111.75(a)(1)(i) | Component - verify identity, dietary ingredient |
| 15927 | 21 CFR 111.103 | Written procedures - quality control operations |
| 15975 | 21 CFR 111.120(e) | Quality control operations - quarantine |