FDA inspection
Aesculap Inc: FDA inspection ending Sep 14, 2016
FDA inspection 986649 · Voluntary Action Indicated (VAI) · Hazelwood, MO
Key facts
| Inspection ID | 986649 |
|---|---|
| Firm | Aesculap Inc |
| FEI number | 3003587896 |
| Address | 615 Lambert Pointe Dr |
| City | Hazelwood |
| State | MO |
| ZIP | 63042 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Sep 14, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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