FDA inspection
Arthrex Gmbh: FDA inspection ending Oct 1, 2015
FDA inspection 960652 · No Action Indicated (NAI) · Munich
Key facts
| Inspection ID | 960652 |
|---|---|
| Firm | Arthrex Gmbh |
| FEI number | 3002579136 |
| Address | Erwin-Hielscher-Str. 9 |
| City | Munich |
| Fiscal year | 2016 |
| Inspection end date | Oct 1, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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