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Dr Reddys gets EIR from USFDA for Srikakulam plant

twitter-logoPTI | February 25, 2018 | Updated 18:57 IST

New Delhi, Feb 25 (PTI) Pharma major Dr Reddys today said it has received the establishment inspection report (EIR) from the US Food and Drug Administration for its its formulations facility in Srikakulam, Andhra Pradesh.

The company, without mentioning the contents of the EIR, said the USFDA has maintained OAI (Official Action Indicated) status at its API manufacturing plant in Srikakulam.

The US drug regulator has asked the company for more details, it said.

"FDA has asked us for more details. We are providing those details and continuing to engage with FDA for resolution of pending issues," Dr Reddys said in a regulatory filing.

An OAI status is equivalent to finding of objectionable conditions at the audit site and also an indicative of regulatory and/or administrative sanctions by FDA.

The USFDA issues an EIR to an establishment that is the subject of an FDA or FDA-contracted inspection when the agency decides to close the inspection.

In April 2017, the company had informed about completion of the audit at its API manufacturing plant in Andhra Pradesh and issuance of two observations by the US drug regulator.

Dr Reddys had said that it was addressing those issues. PTI KPM KPM BAL BAL -

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