FDA inspection
Sanofi Winthrop Industrie: FDA inspection ending Sep 14, 2016
FDA inspection 998080 · Voluntary Action Indicated (VAI) · Aramon
Key facts
| Inspection ID | 998080 |
|---|---|
| Firm | Sanofi Winthrop Industrie |
| FEI number | 3002808341 |
| Address | Route d Avignon |
| City | Aramon |
| Country | France |
| Fiscal year | 2016 |
| Inspection end date | Sep 14, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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