FDA Inspection 989463 — Kee Wah Corporation

Kee Wah Corporation — FEI 3004392931

The FDA completed an inspection of Kee Wah Corporation on September 22, 2016 in South El Monte, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 10 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 22, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
South El Monte, CA (United States)

Citations

IDCFRDescription
128721 CFR 110.20(a)(1)Harborage areas
130621 CFR 110.20(b)(7)Screening
140221 CFR 110.10(b)(4)Unsecured jewelry
140621 CFR 110.10(b)(6)Effective use of hair restraint
155321 CFR 110.35(a)Buildings/good repair
155421 CFR 110.35(a)Cleaning and sanitizing operations
168921 CFR 110.80Reasonable precautions
170121 CFR 110.80(b)(7)Equipment, containers, utensils
176321 CFR 110.35(b)(1)Safe and adequate for use
365221 CFR 110.37(e)(1)Suitable locations