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Dr.Reddy's gets EIR for Miryalaguda plant, indicating closure of USFDA audit

The plant was inspected by USFDA from February 13-21 and had received three Form 483 Observations from US FDA. Miryalaguda plant called at CTO Unit V was one among the three plants.

June 13, 2017 / 22:49 IST
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Dr.Reddy’s on Tuesday said the company has received Establishment Inspection Report (EIR) from US FDA for its active pharmaceutical plant (API) at Miryalaguda indicating the successful closure of the agency’s audit.

“We would now like to inform you that we have received an Establishment Inspection Report (EIR) from US FDA today as closure of audit,” the company said in a statement.

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The plant was inspected by USFDA from February 13-21 got three Form 483 Observations from US FDA.

Miryalaguda plant called at CTO Unit V was one among the three plants for which the company received US drug regulator warning letter in November 2015.