FDA Inspection 1102766 — Shenzhen Shinhop Laser Equipment Co. Ltd.
The FDA completed an inspection of Shenzhen Shinhop Laser Equipment Co. Ltd. on May 21, 2019 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
- May 21, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)