Lupin gets US FDA EIR with satisfactory VAI for Nagpur injectables plant
LUPIN · price
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Lupin Limited received an Establishment Inspection Report (EIR) from the US FDA for its injectables facility in Nagpur, India, classified as Voluntary Action Indicated (VAI) — a satisfactory outcome meaning no regulatory action is needed. The EIR follows an FDA inspection held from September 8 to 16, 2025. Managing Director Nilesh Gupta said the company remains committed to quality and compliance across all facilities.
Positive for shareholders — clears regulatory uncertainty on the Nagpur plant and strengthens confidence in Lupin's US injectables business.