FDA inspection
Rudolf Riester Gmbh: FDA inspection ending Jun 23, 2005
FDA inspection 394775 · No Action Indicated (NAI) · Jungingen
Key facts
| Inspection ID | 394775 |
|---|---|
| Firm | Rudolf Riester Gmbh |
| FEI number | 1000292048 |
| Address | Post Box 35, Bruckstr. 31 |
| City | Jungingen |
| Fiscal year | 2005 |
| Inspection end date | Jun 23, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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