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 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
- May 21, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)