FDA Inspection 1013594 — Waichi Corporation

Waichi Corporation — FEI 3009453065

The FDA completed an inspection of Waichi Corporation on May 18, 2017 in Elkridge, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 18, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Elkridge, MD (United States)

Citations

IDCFRDescription
152421 CFR 123.11(b)Sanitation monitoring
601521 CFR 123.6(c)(6)Verification procedures - none/frequency
601621 CFR 123.6(c)(7)Records system
90821 CFR 123.6(d)Signed and dated
96321 CFR 123.6(c)(5)Corrective action plan