FDA Inspection 1282240 — Unilever Manufacturing (US), Inc.
The FDA completed an inspection of Unilever Manufacturing (US), Inc. on September 15, 2025 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
- September 15, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jonesboro, AR (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1098 | 21 CFR 211.22(c) | Approve or reject procedures or specs |
| 1105 | 21 CFR 211.22(d) | Procedures not in writing, fully followed |
| 1918 | 21 CFR 211.166(a)(2) | Stability sample storage conditions described |
| 4406 | 21 CFR 211.194(a)(2) | Suitability of testing methods verified |
| 4407 | 21 CFR 211.194(a)(2) | Reference and method not stated |
| 4576 | 21 CFR 211.192 | No written record of investigation |