FDA Inspection 764110 — Shenzhen O & E Technologies Co. Ltd.
The FDA completed an inspection of Shenzhen O & E Technologies Co. Ltd. on December 6, 2011 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
- December 6, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)