FDA Inspection 637371 — Okabe Goshikihama Factory

Okabe Goshikihama Factory — FEI 3011288255

The FDA completed an inspection of Okabe Goshikihama Factory on Dec 10, 2009 in Iyo-shi. 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). Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 10, 2009
Fiscal Year
2010
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Iyo-shi (Japan)

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