Attentive Science LLC – FDA 483, Aug 14, 2026

An FDA inspection of Attentive Science LLC, a non-clinical laboratory in Stilwell, KS, revealed numerous significant Good Laboratory Practice (GLP) violations. Findings included inadequate study director oversight, issues with data integrity and accuracy, deficiencies in quality assurance unit operations, and improper handling of test systems, equipment, and archival materials. These observations indicate systemic failures that could compromise the reliability and integrity of nonclinical laboratory studies conducted at the facility.