FDA Inspection 1087904 — Kaneka North America, LLC.

Kaneka North America, LLC. — FEI 3004855873

The FDA completed an inspection of Kaneka North America, LLC. on April 1, 2019 in Pasadena, TX. 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
April 1, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Pasadena, TX (United States)