FDA Inspection 825749 — Universal Orlando Resort

Universal Orlando Resort — FEI 1052415

The FDA completed an inspection of Universal Orlando Resort on Mar 25, 2013 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
Mar 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Orlando, FL (United States)