Mumbai, April 22 -- The USFDA had conducted an inspection of the facility from 2 February 2026 to 6 February 2026. Following the inspection, the regulator issued a Form 483 with one minor observation and classifed the facility under voluntary action indicated status, which the company said has been adequately addressed.

The company said that it remains committed to maintaining full compliance with current Good Manufacturing Practice (cGMP) requirements across all its manufacturing facilities.

Supriya Lifesciences is primarily engaged in manufacturing of bulk drugs and pharmaceutical chemicals.The company's primary focus is to build intermediaries and API for innovators and generic firms. It also exclusively collaborates with partners in...