FDA Inspection 782895 — ADM

ADM — FEI 3003709550

The FDA completed an inspection of ADM on May 8, 2012 in Sabetha, KS. 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
May 8, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Sabetha, KS (United States)

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