FDA Inspection 868921 — GD Group USA Co

GD Group USA Co — FEI 3009542933

The FDA completed an inspection of GD Group USA Co on March 7, 2014 in Bartlett, IL. 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
March 7, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, IL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
317021 CFR 820.198(b)Review and evaluation for investigation