FDA Inspection 715403 — Kesair Technologies, LLC

Kesair Technologies, LLC — FEI 3002959861

The FDA completed an inspection of Kesair Technologies, LLC on February 9, 2011 in Kennesaw, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
312721 CFR 820.80(e)Documentation