This story is from August 16, 2017
USFDA EIR to Granules Gagillapur plant
Hyderabad: City-based pharma player
The company said the USFDA issued no observations for the facility, which manufactures finished dosages and pharmaceutical formulation intermediates. “The USFDA has issued EIR for the Gagillapur facility. This facility was inspected by USFDA in October 2016 and there were no observations during the inspection,” the company said in the regulatory filing.
Granules
India Ltd informed the bourses on Wednesday that it has received the Establishment Inspection Report (EIR) from the US drug watchdog, US Food & Drug Administration, for its Gagillapur facility located in Hyderabad.Popular from Business
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