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 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 30, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Hangzhou (China)