FDA inspection
Siemens Medical Solutions, USA, Inc: FDA inspection ending Feb 2, 2018
FDA inspection 1090599 · No Action Indicated (NAI) · Ann Arbor, MI
Key facts
| Inspection ID | 1090599 |
|---|---|
| Firm | Siemens Medical Solutions, USA, Inc |
| FEI number | 3003304172 |
| Address | 400 W Morgan Rd |
| City | Ann Arbor |
| State | MI |
| ZIP | 48108-9100 |
| Fiscal year | 2018 |
| Inspection end date | Feb 2, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical 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
- 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