Mumbai, March 8 -- In a regulatory filing made after market hours yesterday, the company stated that the United States Food and Drugs Administration (USFDA) had conducted an inspection at Unit-1 of Shilpa Pharma Lifesciences, located at Raichur from March 3-7, 2025.

On conclusion of inspection, we received one observation in form 483, which is procedural in nature.

"The company will closely work with the agency and remain committed to address this observation comprehensively within stipulated time," Shilpa Medicare stated.

Shilpa Medicare is a manufacturer of API, formulation, and development services. Shilpa Medicare (SML) started its operations as an API manufacturer way back in 1987 at Raichur, Karnataka, India.

The company had rep...