FDA Inspection 1142240 — Synthite USA, Inc.

Synthite USA, Inc. — FEI 3012439994

The FDA completed an inspection of Synthite USA, Inc. on May 20, 2021 in Oak Park, IL. 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
May 20, 2021
Fiscal Year
2021
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Oak Park, IL (United States)

Additional Details

FSVP