FDA Inspection 982044 — KUKI SANGYO CO., LTD. Takenari Factory

KUKI SANGYO CO., LTD. Takenari Factory — FEI 3004666154

The FDA completed an inspection of KUKI SANGYO CO., LTD. Takenari Factory on Aug 4, 2016 in Mie-Gun. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 4, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Mie-Gun (Japan)

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