FDA inspection
SunMed AP, Ltd.: FDA inspection ending Mar 31, 2016
FDA inspection 977038 · No Action Indicated (NAI) · Zhuhai
Key facts
| Inspection ID | 977038 |
|---|---|
| Firm | SunMed AP, Ltd. |
| FEI number | 3005998497 |
| Address | Qianwu Industry Park, Doume District |
| City | Zhuhai |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Mar 31, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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