FDA Inspection 921811 — ADM Europoort BV

ADM Europoort BV — FEI 2000035609

The FDA completed an inspection of ADM Europoort BV on Feb 16, 2015 in Europoort Rotterdam. 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
Feb 16, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Europoort Rotterdam (Netherlands)

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