FDA Inspection 1035848 — IQ Technologies, Inc.

IQ Technologies, Inc. — FEI 3008806536

The FDA completed an inspection of IQ Technologies, Inc. on Dec 12, 2017 in Las Vegas, NV. 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
Dec 12, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Las Vegas, NV (United States)