FDA Inspection 1065602 — SHENZHEN TSD LASER EQUIPMENT CO., LTD.
The FDA completed an inspection of SHENZHEN TSD LASER EQUIPMENT CO., LTD. on Dec 6, 2017 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
- Dec 6, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)