FDA Inspection 921811 — ADM Europoort BV
The FDA completed an inspection of ADM Europoort BV on February 16, 2015 in Europoort Rotterdam. 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
- February 16, 2015
- Fiscal Year
- 2015
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Europoort Rotterdam (Netherlands)