FDA Inspection 1102021 — BIAOKE LASER TECHNOLOGY (HANGZHOU) CO., LTD.
The FDA completed an inspection of BIAOKE LASER TECHNOLOGY (HANGZHOU) CO., LTD. on May 30, 2019 in Hangzhou. 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 30, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Hangzhou (China)