FDA Inspection 972695 — Carwild Corporation

Carwild Corporation — FEI 1219313

The FDA completed an inspection of Carwild Corporation on June 3, 2016 in New London, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 3, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
New London, CT (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
341521 CFR 820.22Quality Audit/Reaudit - conducted
369621 CFR 820.100(b)Documentation