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Glenmark Goa Plant Gets VAI Status from US FDA

Glenmark Goa Plant Gets VAI Status from US FDA

Glenmark Pharmaceuticals has received the Establishment Inspection Report (EIR) from the US Food and Drug Administration (FDA) for its formulations manufacturing facility in Goa, India with a Voluntary Action Indicated (VAI) status.

The inspection was conducted at the company’s manufacturing facility from June 22, 2026 to June 30, 2026.
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Glenmark Establishment Inspection Report Glenmark formulations facility Glenmark Goa facility Glenmark Pharmaceuticals Glenmark US FDA inspection Pharmaceutical manufacturing Goa Voluntary Action Indicated
More news about: regulation | Published by News Bureau | September - 23 - 2026

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