FDA Inspection 950532 — Miyoshi America, Inc

Miyoshi America, Inc — FEI 3009481791

The FDA completed an inspection of Miyoshi America, Inc on Nov 17, 2015 in Dayville, CT. 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
Nov 17, 2015
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Dayville, CT (United States)

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