FDA inspection
Siemans Medial Solutions USA, Inc: FDA inspection ending Apr 13, 2017
FDA inspection 1025561 · Voluntary Action Indicated (VAI) · Plymouth Meeting, PA
Key facts
| Inspection ID | 1025561 |
|---|---|
| Firm | Siemans Medial Solutions USA, Inc |
| FEI number | 3002626007 |
| Address | 5168 Campus Dr |
| City | Plymouth Meeting |
| State | PA |
| ZIP | 19462-1123 |
| Fiscal year | 2017 |
| Inspection end date | Apr 13, 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
- 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