FDA inspection
Sanofi Winthrop Industrie: FDA inspection ending Apr 30, 2010
FDA inspection 665406 · Voluntary Action Indicated (VAI) · Vitry-Sur-Seine
Key facts
| Inspection ID | 665406 |
|---|---|
| Firm | Sanofi Winthrop Industrie |
| FEI number | 3002808000 |
| Address | Centre de Production de Vitry, 9 quai Jules Guesde |
| City | Vitry-Sur-Seine |
| Country | France |
| Fiscal year | 2010 |
| Inspection end date | Apr 30, 2010 |
| 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
- 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