FDA Inspection 894778 — Lee Laser, Inc.
The FDA completed an inspection of Lee Laser, Inc. on Sep 10, 2014 in Orlando, FL. 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
- Sep 10, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Orlando, FL (United States)