Westwood Laboratories, LLC. – FDA 483, May 30, 2019

Westwood Laboratories, Inc. in Azusa, CA, received a Form 483 citing three observations related to laboratory controls and data integrity during an inspection from May 13-30, 2019. The observations highlight issues with computer system controls, including lack of user roles and data discrepancies, as well as inadequate microbiological testing procedures and unauthorized retesting of drug products. These findings indicate significant concerns regarding the firm's quality control and data management practices.