FDA Inspection 1195519 — IQ Technologies, Inc.

IQ Technologies, Inc. — FEI 3008806536

The FDA completed an inspection of IQ Technologies, Inc. on Jan 10, 2023 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
Jan 10, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Las Vegas, NV (United States)