FDA Inspection 942794 — Unilever Manufacturing (US), Inc.
The FDA completed an inspection of Unilever Manufacturing (US), Inc. on July 10, 2015 in Jonesboro, AR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 10, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jonesboro, AR (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1213 | 21 CFR 211.67(a) | Cleaning / Sanitizing / Maintenance |
| 1943 | 21 CFR 211.180(e)(1) | Review of representative number of batches |
| 3445 | 21 CFR 211.65(a) | Equipment construction - reactive surfaces |
| 3559 | 21 CFR 211.56(a) | Sanitation--buildings not clean, free of infestation |
| 4315 | 21 CFR 211.84(d)(2) | Testing Each Component for Conformity with Specs |
| 4340 | 21 CFR 211.142 | Written warehousing procedures established/followed |