483
Archer Daniels Midland CompanyArcher Daniels Midland Company – FDA 483, Aug 22, 2025
Record Details
Archer-Daniels-Midland Company in Des Moines, IA, received a Form 483 following an inspection of its Type A medicated article facility. Observations included inadequate control over expiration dating for medicated articles, issues with preventing mix-ups during packaging and labeling, and insufficient verification of label quantities. These findings indicate deficiencies in quality control and adherence to good manufacturing practices.
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