FDA Inspection 1027009 — Guangdong Baihe Medical Technology Co., Ltd
The FDA completed an inspection of Guangdong Baihe Medical Technology Co., Ltd on August 24, 2017 in Foshan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- August 24, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Foshan (China)