FDA Inspection 808962 — Kuki Sangyo Co., Ltd.

Kuki Sangyo Co., Ltd. — FEI 1000272783

The FDA completed an inspection of Kuki Sangyo Co., Ltd. on Nov 22, 2012 in Yokkaichi. 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). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 22, 2012
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Yokkaichi (Japan)

Citations

IDCFRDescription
159921 CFR 110.37(b)(5)Backflow prevention
169821 CFR 110.80(b)(5)Work-in-progress

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