FDA inspection
Ge Healthcare (Tianjin) Company: FDA inspection ending May 25, 2017
FDA inspection 1015943 · No Action Indicated (NAI) · Dongli
Key facts
| Inspection ID | 1015943 |
|---|---|
| Firm | Ge Healthcare (Tianjin) Company |
| FEI number | 3010949642 |
| Address | Tianjin Konggang Wuliujiagong Qu, Dongli |
| City | Dongli |
| Country | China |
| Fiscal year | 2017 |
| Inspection end date | May 25, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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