FDA Inspection 999620 — AED Enterprises LLC

AED Enterprises LLC — FEI 3008067944

The FDA completed an inspection of AED Enterprises LLC on December 21, 2016 in Cincinnati, OH. 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
December 21, 2016
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Cincinnati, OH (United States)

Citations

IDCFRDescription
100621 CFR 110.10(b)(8)Personal food/drink/tobacco
140521 CFR 110.10(b)(6)Failure to wear
364321 CFR 110.10(b)(5)Glove condition