FDA Inspection 775617 — Guangdong Baihe Medical Technology Co., Ltd
The FDA completed an inspection of Guangdong Baihe Medical Technology Co., Ltd on March 30, 2012 in Foshan. 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
- March 30, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Foshan (China)