USFDA issues EIR for Granules India's Gagillapur plant

Press Trust of India  |  New Delhi 

Drug firm today said the US health regulator has issued establishment inspection report for its Gagillapur plant in without any observations.

The United States Food and Drug Administration (USFDA) has issued establishment inspection report (EIR) for the company's Gagillapur facility in Hyderabad, said in a regulatory filing.


"The facility was inspected by the USFDA in October 2016 and there were no observations during the inspection", it added.

Finished dosages and pharmaceutical formulation intermediates are manufactured at the plant, it said.

stock was trading nearly 8 per cent up at Rs 125.75 on in the afternoon.

(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)