Mumbai, May 26 -- In a regulatory filing made on Saturday (24 May 2025), the company informed that the US FDA had conducted a GMP inspection at its API manufacturing facility in Miryalaguda, Telangana, India. The inspection was conducted from 19 May 2025 to 24 May 2025.

Post the inspection, the American regulatory agency has issued a Form 483 with 2 observations.

The pharmaceutical company stated that it would address the said observation from the US FDA within the stipulated timeline.

Hyderabad-based Dr. Reddy's Laboratories is a global pharmaceutical company. It offers a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC.

The company reported a consolidated net profit of Rs 1,594 crore...