FDA inspection
Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH: FDA inspection ending Nov 27, 2014
FDA inspection 909450 · No Action Indicated (NAI) · Duderstadt
Key facts
| Inspection ID | 909450 |
|---|---|
| Firm | Ottobock SE & Co. KGaA Formerly Known As Otto Bock Healthcare GmbH |
| FEI number | 3003117657 |
| Address | Max-Nader-Str. # 15 |
| City | Duderstadt |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Nov 27, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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