FDA Inspection 926689 — Guangzhou Berrcom Medical Device Co., Ltd
The FDA completed an inspection of Guangzhou Berrcom Medical Device Co., Ltd on Apr 30, 2015 in Guangzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 30, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Guangzhou (China)