FDA Inspection 1267100 — QED, Inc.

QED, Inc. — FEI 1037039

The FDA completed an inspection of QED, Inc. on April 11, 2025 in Lexington, KY. 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
April 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lexington, KY (United States)

Citations

IDCFRDescription
2279521 CFR 801.20(a)Label to bear a unique device identifier
2280021 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.