FDA Inspection 1037082 — Aker BioMarine Manufacturing LLC

Aker BioMarine Manufacturing LLC — FEI 3010865990

The FDA completed an inspection of Aker BioMarine Manufacturing LLC on December 14, 2017 in Houston, 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
December 14, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Houston, TX (United States)