FDA 483 - AmerisourceBergen Drug Corporation - March 07, 2019

AmerisourceBergen Drug Corporation in Buford, GA, was inspected by the FDA from March 5-7, 2019. The inspection revealed that the firm did not routinely calibrate its automated, mechanical, or electronic equipment. Specifically, temperature and humidity recording equipment had not been calibrated since January 2018, violating the firm's own established policy.