Divis Laboratories receives EIR for Visakhapatnam unit

18 Nov 2017 Evaluate

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.

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