FDA inspection
Sanofi Winthrop Industrie: FDA inspection ending Feb 18, 2020
FDA inspection 1120933 · Voluntary Action Indicated (VAI) · Lyon
Key facts
| Inspection ID | 1120933 |
|---|---|
| Firm | Sanofi Winthrop Industrie |
| FEI number | 3009194033 |
| Address | 23 boulevard Chambaud de la Bruyere |
| City | Lyon |
| Country | France |
| Fiscal year | 2020 |
| Inspection end date | Feb 18, 2020 |
| 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
- 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