US Food and Drug Administration (USFDA) has completed inspection at Divi’s Laboratories’ Unit-II, Village Chippada, Bheemunipatnam District in the state of Andhra Pradesh. The inspection was conducted from January 27 to 31, 2020. The inspection has been concluded with no ‘483’ observations.
Divis Laboratories focussed on developing new processes for the production of Active Pharma Ingredients (APIs) & Intermediates. The company in a matter of short time expanded its breadth of operations to provide complete turnkey solutions to the domestic Indian pharmaceutical industry.