FDA Inspection 1284704 — ADM Crosswind

ADM Crosswind — FEI 3010743565

The FDA completed an inspection of ADM Crosswind on June 2, 2026 in Topeka, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 2, 2026
Fiscal Year
2026
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Topeka, KS (United States)

Citations

IDCFRDescription
1821921 CFR 507.25(b)(1)Raw Material Controls