FDA Inspection 1122854 — Wuhan Sunic Photoelectricity Equipment Manufacture Co. Ltd.
The FDA completed an inspection of Wuhan Sunic Photoelectricity Equipment Manufacture Co. Ltd. on December 9, 2019 in Wuhan. 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
- December 9, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Wuhan (China)