FDA inspection
WuJiang City ShenLing Medical Device Co., Ltd.: FDA inspection ending Sep 1, 2011
FDA inspection 749485 · Voluntary Action Indicated (VAI) · Suzhou
Key facts
| Inspection ID | 749485 |
|---|---|
| Firm | WuJiang City ShenLing Medical Device Co., Ltd. |
| FEI number | 3003255801 |
| Address | Building 18, Beishe Street; Wujiang |
| City | Suzhou |
| Country | China |
| Fiscal year | 2011 |
| Inspection end date | Sep 1, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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