FDA inspection
Sanofi - Aventis US LLC: FDA inspection ending Jun 17, 2005
FDA inspection 384457 · Voluntary Action Indicated (VAI) · Kansas City, MO
Key facts
| Inspection ID | 384457 |
|---|---|
| Firm | Sanofi - Aventis US LLC |
| FEI number | 1913298 |
| Address | 10236 Marion Park Dr |
| City | Kansas City |
| State | MO |
| ZIP | 64137-1405 |
| Fiscal year | 2005 |
| Inspection end date | Jun 17, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
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