FDA inspection
Siemens Healthcare Diagnostics Inc.: FDA inspection ending Sep 13, 2012
FDA inspection 799832 · Voluntary Action Indicated (VAI) · Brookfield, CT
Key facts
| Inspection ID | 799832 |
|---|---|
| Firm | Siemens Healthcare Diagnostics Inc. |
| FEI number | 3002755490 |
| Address | 101 Silvermine Rd |
| City | Brookfield |
| State | CT |
| ZIP | 06804 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Sep 13, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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