Archive · 23 Sep 2026

Glenmark Goa Facility Receives VAI Status After FDA Inspection

Glenmark Goa Facility Receives VAI Status After FDA Inspection

Glenmark makes medicines at a factory in Goa.

The US Food and Drug Administration inspected that factory.

The inspection happened from June 22 to June 30.

The FDA gave the factory a report called an Establishment Inspection Report.

It classified the inspection as Voluntary Action Indicated, or VAI.

This means the FDA saw some issues but did not recommend formal regulatory action.

Glenmark is expected to address the issues voluntarily.

The company did not say exactly what the issues or fixes were, and its shares rose slightly after the announcement.

Sources