FDA inspection
VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG.: FDA inspection ending Apr 26, 2007
FDA inspection 471095 · No Action Indicated (NAI) · Bad Sackingen
Key facts
| Inspection ID | 471095 |
|---|---|
| Firm | VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG. |
| FEI number | 4838 |
| Address | Spitalgasse 3 |
| City | Bad Sackingen |
| Fiscal year | 2007 |
| Inspection end date | Apr 26, 2007 |
| 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