FDA inspection
Siemens Healthcare Diagnostics Products GmbH: FDA inspection ending Mar 26, 2009
FDA inspection 573266 · Voluntary Action Indicated (VAI) · Marburg
Key facts
| Inspection ID | 573266 |
|---|---|
| Firm | Siemens Healthcare Diagnostics Products GmbH |
| FEI number | 3001644026 |
| Address | Emil-von-behring-str. 76 |
| City | Marburg |
| Country | Germany |
| Fiscal year | 2009 |
| Inspection end date | Mar 26, 2009 |
| 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