FDA inspection
GE Hangwei Medical Systems, Co. Ltd.: FDA inspection ending Dec 12, 2017
FDA inspection 1038962 · No Action Indicated (NAI) · Beijing
Key facts
| Inspection ID | 1038962 |
|---|---|
| Firm | GE Hangwei Medical Systems, Co. Ltd. |
| FEI number | 3002175190 |
| Address | West Area, Bldg. 3, Beijing Economic Dev. Area, 1 Yongchangbeilu; |
| City | Beijing |
| Country | China |
| Fiscal year | 2018 |
| Inspection end date | Dec 12, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Radiation Control and Health Safety Act |
| 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