FDA inspection
Unilever Manufacturing (US), Inc.: FDA inspection ending Feb 7, 2013
FDA inspection 830505 · Sikeston, MO
Key facts
| Inspection ID | 830505 |
|---|---|
| Firm | Unilever Manufacturing (US), Inc. |
| FEI number | 3002915882 |
| Address | 2400 Rose Pkwy |
| City | Sikeston |
| State | MO |
| ZIP | 63801-7192 |
| Fiscal year | 2013 |
| Inspection end date | Feb 7, 2013 |
| 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
- 10–99 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