FDA inspection
Zhejiang Kindly Medical Devices Co., Ltd.: FDA inspection ending Mar 25, 2015
FDA inspection 920219 · No Action Indicated (NAI) · Wenzhou
Key facts
| Inspection ID | 920219 |
|---|---|
| Firm | Zhejiang Kindly Medical Devices Co., Ltd. |
| FEI number | 3003560965 |
| Address | # 758 Binghai Five Rd., Longwan Dist |
| City | Wenzhou |
| Country | China |
| Fiscal year | 2015 |
| Inspection end date | Mar 25, 2015 |
| 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