FDA inspection
Siemens Medical Solutions USA, Inc.: FDA inspection ending Apr 6, 2017
FDA inspection 1022705 · Voluntary Action Indicated (VAI) · Mountain View, CA
Key facts
| Inspection ID | 1022705 |
|---|---|
| Firm | Siemens Medical Solutions USA, Inc. |
| FEI number | 2936884 |
| Address | 685 E Middlefield Rd |
| City | Mountain View |
| State | CA |
| ZIP | 94043-4045 |
| Fiscal year | 2017 |
| Inspection end date | Apr 6, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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