FDA Inspection 950532 — Miyoshi America, Inc

Miyoshi America, Inc — FEI 3009481791

The FDA completed an inspection of Miyoshi America, Inc on November 17, 2015 in Dayville, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 17, 2015
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Dayville, CT (United States)