FDA Inspection 1036153 — Unimicro Medical Systems (Shenzhen) Co., Ltd.
The FDA completed an inspection of Unimicro Medical Systems (Shenzhen) Co., Ltd. on November 9, 2017 in Shenzhen. 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
- November 9, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)