FDA Inspection 1029019 — ARCHER DANIELS MIDLAND

ARCHER DANIELS MIDLAND — FEI 3004052274

The FDA completed an inspection of ARCHER DANIELS MIDLAND on Jul 11, 2017 in Quincy, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 11, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Quincy, IL (United States)

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