FDA Inspection 1221624 — Shenzhen Dapeng Laser Technology Co., Ltd.
The FDA completed an inspection of Shenzhen Dapeng Laser Technology Co., Ltd. on September 8, 2023 in Shenzhen. 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
- September 8, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)