FDA inspection
Stork Instrumente GmbH: FDA inspection ending Feb 25, 2015
FDA inspection 921478 · No Action Indicated (NAI) · Emmingen-Liptingen
Key facts
| Inspection ID | 921478 |
|---|---|
| Firm | Stork Instrumente GmbH |
| FEI number | 1000168975 |
| Address | Engener Str. 29 |
| City | Emmingen-Liptingen |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Feb 25, 2015 |
| 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