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Shilpa Medicare gets EIR from USFDA for Jadcherla facility

Press Trust of India  |  New Delhi 

today said the USFDA has issued an Establishment Inspection Report (EIR) for its Jadcherla facility in

The US health regulator has issued an EIR for the company's generic pharmaceutical manufacturing facility at Jadcherla, which was inspected between July 24-28, 2017, said in a filing to


The inspection has now been closed by the USFDA, it added.

"The company had submitted a detailed corrective and preventive action (CAPA) plan to the regulator within the stipulated timelines in response to the form 483 issued at the end of inspection," it said.

The USFDA has reviewed the CAPA and found it acceptable, it added.

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

First Published: Sat, October 07 2017. 14:13 IST
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