FDA Inspection 1034030 — Kwong Yet Lung Company

Kwong Yet Lung Company — FEI 3000719305

The FDA completed an inspection of Kwong Yet Lung Company on November 30, 2017 in Las Vegas, NV. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 30, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Las Vegas, NV (United States)

Citations

IDCFRDescription
152421 CFR 123.11(b)Sanitation monitoring
1816521 CFR 117.93Storage and Distribution
600821 CFR 123.8(a)(3)Verification - record review - frequency
601621 CFR 123.6(c)(7)Records system
601821 CFR 123.7(a)Corrective action per predetermined plan
90521 CFR 123.6(b)HACCP plan implementation