FDA inspection
RM Temena GmbH: FDA inspection ending Feb 27, 2014
FDA inspection 871224 · Voluntary Action Indicated (VAI) · Felsberg
Key facts
| Inspection ID | 871224 |
|---|---|
| Firm | RM Temena GmbH |
| FEI number | 3005379387 |
| Address | Mittelhoefer Str. 1, D-34587 |
| City | Felsberg |
| Country | Germany |
| Fiscal year | 2014 |
| Inspection end date | Feb 27, 2014 |
| 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