FDA Inspection 912667 — APK Technology Co., Ltd.
The FDA completed an inspection of APK Technology Co., Ltd. on February 3, 2015 in Shenzhen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- February 3, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)