FDA Inspection 1278067 — Shenzhen Optlaser Technologies Co. Ltd.
The FDA completed an inspection of Shenzhen Optlaser Technologies Co. Ltd. on Jun 5, 2025 in Shenzhen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 5, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)