FDA inspection
Unilever Manufacturing (US), Inc.: FDA inspection ending Sep 27, 2001
FDA inspection 89347 · Voluntary Action Indicated (VAI) · Jonesboro, AR
Key facts
| Inspection ID | 89347 |
|---|---|
| Firm | Unilever Manufacturing (US), Inc. |
| FEI number | 3006642851 |
| Address | 2407 Quality Way |
| City | Jonesboro |
| State | AR |
| ZIP | 72401-9264 |
| Fiscal year | 2001 |
| Inspection end date | Sep 27, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Colors and Cosmetics Technology |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data