Lupin receives US FDA EIR with VAI classification for Goa facility
Inspection conducted in November 2025; Establishment Inspection Report issued by US regulator
Lupin has announced that it has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (US FDA) for its facility in Goa, India, with a Voluntary Action Indicated (VAI) classification. The EIR was issued following an inspection of the facility conducted from November 10 to November 21, 2025.
Nilesh Gupta, Managing Director, Lupin, stated, “We are pleased to have received the EIR with a VAI classification from the US FDA for our Goa facility. This outcome reflects our continued focus on quality excellence and regulatory compliance, reinforcing our commitment to delivering safe and effective medicines to patients worldwide.”