FDA Inspection 1101181 — HQ, Inc.

HQ, Inc. — FEI 1038689

The FDA completed an inspection of HQ, Inc. on August 30, 2019 in Palmetto, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 30, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Palmetto, FL (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
316021 CFR 820.184Lack of or inadequate DHR procedures