FDA inspection
Arthrex Medizinische Instrumente GmbH: FDA inspection ending Oct 2, 2015
FDA inspection 960647 · Voluntary Action Indicated (VAI) · Odelzhausen
Key facts
| Inspection ID | 960647 |
|---|---|
| Firm | Arthrex Medizinische Instrumente GmbH |
| FEI number | 3007193505 |
| Address | Oskar-von-Miller-Str. 6 |
| City | Odelzhausen |
| Fiscal year | 2016 |
| Inspection end date | Oct 2, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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
- 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