FDA Inspection 1094832 — AED Enterprises Inc

AED Enterprises Inc — FEI 3008047296

The FDA completed an inspection of AED Enterprises Inc on June 26, 2019 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 8 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 26, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
1814121 CFR 117.35(a)Sanitary operations - Plant maintenance
1814221 CFR 117.35(a)Sanitary operations - Plant sanitation
1814521 CFR 117.35(c)Pest control
1814721 CFR 117.35(e)Sanitation of non-food-contact surfaces - Manner and frequency
1814821 CFR 117.37Sanitary facilities and controls
1814921 CFR 117.40Equipment and utensils - Design and maintenance
1839721 CFR 117.4Qualifications of individuals
1902721 CFR 117.126(a)(1)Food safety plan