FDA inspection
Zhejiang Gongdong Medical Technology Co., Ltd: FDA inspection ending May 22, 2014
FDA inspection 882603 · No Action Indicated (NAI) · Taizhou
Key facts
| Inspection ID | 882603 |
|---|---|
| Firm | Zhejiang Gongdong Medical Technology Co., Ltd |
| FEI number | 3005739529 |
| Address | 10 and 39 Beiyuan Ave, Economic Development Zone |
| City | Taizhou |
| Country | China |
| Fiscal year | 2014 |
| Inspection end date | May 22, 2014 |
| 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