FDA inspection
GFA Production Xiamen Co., Ltd.: FDA inspection ending Sep 26, 2013
FDA inspection 851259 · Voluntary Action Indicated (VAI) · Xiamen
Key facts
| Inspection ID | 851259 |
|---|---|
| Firm | GFA Production Xiamen Co., Ltd. |
| FEI number | 3008384335 |
| Address | Huli Industrial Park, Tong'an District, 20 Meixi Avenue |
| City | Xiamen |
| Country | China |
| Fiscal year | 2013 |
| Inspection end date | Sep 26, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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