Divis Laboratories has received an Establishment Inspection Report (EIR) from the United States Food & Drug Administration (USFDA) for its Unit-II, located at Visakhapatnam, Andhra Pradesh, as closure of audit by USFDA.
Earlier in September, the company's Unit-II was inspected by USFDA wherein a Form-483 was issued with 6 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.