"The company has received the Establishment Inspection Report (EIR) after the closure of the US Food and Drug Administration (USFDA) inspection of its Mandideep Unit II facility, classifying the inspection as Voluntary Action Indicated (VAI). The inspection at the facility was carried out by the US.FDA between November 26, 2018 and December 4, 2018," the company said.
On Monday, April 13, Lupin had received an EIR from the US health regulator for its manufacturing plant in Nagpur. While, earlier this month, the drug major said its Aurangabad facility received EIR report from the USFDA.
At 10:32 am, Lupin was up 1 per cent at Rs 837 on the BSE, as against a 2.7 per cent rise in the S&P BSE Sensex. A combined 2.3 million shares have changed hands on the counter on the NSE and BSE till the time of writing of this report.
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