FDA inspection
Reda Instrumente Gmbh: FDA inspection ending Jun 13, 2013
FDA inspection 840343 · No Action Indicated (NAI) · Tuttlingen
Key facts
| Inspection ID | 840343 |
|---|---|
| Firm | Reda Instrumente Gmbh |
| FEI number | 3002807988 |
| Address | Gansacker 34 |
| City | Tuttlingen |
| Country | Germany |
| Fiscal year | 2013 |
| Inspection end date | Jun 13, 2013 |
| 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