FDA Inspection 805763 — Ultralite Enterprises Inc
The FDA completed an inspection of Ultralite Enterprises Inc on Nov 1, 2012 in Dacula, GA. 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
- Nov 1, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Dacula, GA (United States)