FDA 483 - Vege Labs LLC - March 18, 2025

Vege Labs LLC, a drug manufacturer in Glendale, CA, was inspected by the FDA and received a Form 483. The inspection revealed significant deficiencies including inadequate component testing, failure to investigate out-of-specification results, poor computer system controls, and a lack of proper cleaning validation for equipment. These issues indicate a lack of adherence to good manufacturing practices, potentially impacting drug product quality and safety.