FDA Inspection 1084854 — Shenzhen Poda Laser Technology Co. Ltd.
The FDA completed an inspection of Shenzhen Poda Laser Technology Co. Ltd. on Oct 31, 2018 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
- Oct 31, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)