FDA Inspection 1068987 — Max Plus Laser Co. Ltd.
The FDA completed an inspection of Max Plus Laser Co. Ltd. on May 25, 2017 in Zhongshan. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 25, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Zhongshan (China)