FDA inspection
Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.: FDA inspection ending Aug 26, 2010
FDA inspection 683815 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 683815 |
|---|---|
| Firm | Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. |
| FEI number | 3004173703 |
| Address | Bldg 1 F/3-6, National Highway 107, Xixiang, Baoan |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2010 |
| Inspection end date | Aug 26, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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