Lupin receives EIR from USFDA for Goa facility
The EIR was issued following an inspection of the facility from November 10 to November 21, 2025
Lupin has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for its facility in Goa, India, with a satisfactory Voluntary Action Indicated (VAI) classification. The EIR was issued following an inspection of the facility from November 10 to November 21, 2025.
Lupin is an innovation led transnational pharmaceutical company producing, developing and marketing a wide range of branded and generic formulations, biotechnology products and active pharmaceutical ingredients (APIs) globally.
