FDA inspection
Siemens Healthineers Ltd.: FDA inspection ending Sep 17, 2012
FDA inspection 802825 · Voluntary Action Indicated (VAI) · Pohang-Si
Key facts
| Inspection ID | 802825 |
|---|---|
| Firm | Siemens Healthineers Ltd. |
| FEI number | 3006985147 |
| Address | 2nd & 3rd Venture Bld., 394, Jigok-ro, Pohan Technopark |
| City | Pohang-Si |
| Country | Korea (the Republic of) |
| Fiscal year | 2012 |
| Inspection end date | Sep 17, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| 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