FDA inspection
ROSE GMBH FUER MEDIZINTECHNIK: FDA inspection ending Nov 13, 2008
FDA inspection 550670 · Voluntary Action Indicated (VAI) · Trier
Key facts
| Inspection ID | 550670 |
|---|---|
| Firm | ROSE GMBH FUER MEDIZINTECHNIK |
| FEI number | 3002808022 |
| Address | D-54294, D-54294 |
| City | Trier |
| Country | Germany |
| Fiscal year | 2009 |
| Inspection end date | Nov 13, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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