FDA Inspection 1080540 — Shenzhen Biocare Bio-Medical Equipment Co., Ltd.
The FDA completed an inspection of Shenzhen Biocare Bio-Medical Equipment Co., Ltd. on Jan 24, 2019 in Shenzhen. 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
- Jan 24, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)