FDA inspection
APK Technology Co., Ltd.: FDA inspection ending Feb 3, 2015
FDA inspection 912667 · Official Action Indicated (OAI) · Shenzhen
Key facts
| Inspection ID | 912667 |
|---|---|
| Firm | APK Technology Co., Ltd. |
| FEI number | 3007699081 |
| Address | 601, 6 Floor, C6 Building, Industry Of Hengfeng, Hezhou, Xixian; Baoan |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2015 |
| Inspection end date | Feb 3, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
| Warning letter | 460945 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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