USFDA issues EIR with Voluntary Action Indicated for Lupin's Somerset facility
Lupin announced that it has received the Establishment Inspection Report (EIR) from United States Food and Drug Administration (US FDA) for its Somerset, NJ manufacturing facility, after the inspection of the facility
in March 2022. The US FDA has determined that the inspection classification of the facility is Voluntary Action Indicated (VAI).
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First Published: Jul 07 2022 | 9:17 AM IST