FDA Inspection 895771 — HIQ Solutions Group
The FDA completed an inspection of HIQ Solutions Group on Aug 27, 2014 in Miami, 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
- Aug 27, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Miami, FL (United States)