FDA inspection
Sanofi Winthrop Industrie: FDA inspection ending Nov 4, 2011
FDA inspection 753776 · No Action Indicated (NAI) · Carbon Blanc CEDEX
Key facts
| Inspection ID | 753776 |
|---|---|
| Firm | Sanofi Winthrop Industrie |
| FEI number | 3002808208 |
| Address | Sanofi, 1 rue de la Vierge; Ambares Et Lagrave |
| City | Carbon Blanc CEDEX |
| Country | France |
| Fiscal year | 2012 |
| Inspection end date | Nov 4, 2011 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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