FDA Inspection 1120502 — Unilever Manufacturing (US), Inc.
The FDA completed an inspection of Unilever Manufacturing (US), Inc. on March 10, 2020 in Jonesboro, AR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 10, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jonesboro, AR (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1105 | 21 CFR 211.22(d) | Procedures not in writing, fully followed |
| 4402 | 21 CFR 211.192 | Written record of investigation incomplete |