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Dr Reddy's Lab gets EIR from USFDA for Vizag units

Press Trust of India  |  New Delhi 

Dr Reddy's Laboratories on Thursday said it has received establishment inspection report (EIR) from the US health regulator for its Visakhapatnam facility in Andhra Pradesh.

The company has received EIR from the United States Food and Drug Administration (USFDA) for the inspection conducted at the formulations manufacturing plants at Duvvada Visakhapatnam, Dr Reddy's Laboratories said in a regulatory filing.

The inspection of the two facilities were completed by the USFDA on June 21 this year, it added.

"We have now received an EIR from the USFDA, indicating closure of this audit," the company said.

The USFDA gives EIR on closure of inspection of an establishment that is the subject of an USFDA or USFDA-contracted inspection.

Dr Reddy's shares on Thursday ended 0.13 per cent up at Rs 2,765.30 apiece on the BSE.

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

First Published: Thu, September 12 2019. 19:35 IST
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