FDA Inspection 1034030 — Kwong Yet Lung Company

Kwong Yet Lung Company — FEI 3000719305

The FDA completed an inspection of Kwong Yet Lung Company on Nov 30, 2017 in Las Vegas, NV. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.