FDA Inspection 831102 — Intermex Products USA, Ltd

Intermex Products USA, Ltd — FEI 1640978

The FDA completed an inspection of Intermex Products USA, Ltd on May 3, 2013 in Grand Prairie, TX. 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: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 3, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Grand Prairie, TX (United States)

Citations

IDCFRDescription
161521 CFR 110.93Storage/transportation of finished goods (contamination)
164021 CFR 113.100(b)Record form not signed
169821 CFR 110.80(b)(5)Work-in-progress