FDA Inspection 1118942 — QED, Inc.

QED, Inc. — FEI 1037039

The FDA completed an inspection of QED, Inc. on Feb 26, 2020 in Lexington, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 26, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
337521 CFR 820.198(e)Records of complaint investigation

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