FDA inspection
Siemens Healthcare Diagnostics: FDA inspection ending May 12, 2006
FDA inspection 424931 · No Action Indicated (NAI) · Los Angeles, CA
Key facts
| Inspection ID | 424931 |
|---|---|
| Firm | Siemens Healthcare Diagnostics |
| FEI number | 3005250747 |
| Address | 5210 Pacific Concourse Dr |
| City | Los Angeles |
| State | CA |
| ZIP | 90045-6900 |
| Fiscal year | 2006 |
| Inspection end date | May 12, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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
- 10–99 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