FDA Inspection 1027148 — Suzhou Suntop Laser Technology Co. Ltd.
The FDA completed an inspection of Suzhou Suntop Laser Technology Co. Ltd. on June 7, 2017 in Suzhou. 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
- June 7, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Suzhou (China)