FDA inspection
Sanofi Winthrop Industrie: FDA inspection ending Mar 30, 2012
FDA inspection 779441 · Voluntary Action Indicated (VAI) · Ploermel
Key facts
| Inspection ID | 779441 |
|---|---|
| Firm | Sanofi Winthrop Industrie |
| FEI number | 3005224144 |
| Address | Zone Industrielle du Bois Vert, rue Gilles Roberval |
| City | Ploermel |
| Country | France |
| Fiscal year | 2012 |
| Inspection end date | Mar 30, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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