FDA Inspection 999219 — LiquidCapsule Manufacturing, LLC
The FDA completed an inspection of LiquidCapsule Manufacturing, LLC on Oct 28, 2016 in Tampa, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 6 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 28, 2016
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Tampa, FL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15380 | 21 CFR 111.8 | Written procedures - sick or infected personnel |
| 15444 | 21 CFR 111.15(c)(1) | Cleaning compounds |
| 15532 | 21 CFR 111.255(b) | Batch record - complete |
| 15675 | 21 CFR 111.315(b) | Sampling plans; establish, follow |
| 15723 | 21 CFR 111.365(i) | Metal, foreign material |
| 15986 | 21 CFR 111.123(b)(2) | Quality control - batch, product specifications |