Dr. Reddy’s Laboratories has announced that the United States Food & Drug Administration (USFDA) has completed a comprehensive GMP and Pre-Approval Inspection (PAI) at its formulations facility, FTO-SEZ PU01, located in Srikakulam, Andhra Pradesh. The inspection took place between 4 December and 12 December 2025 and concluded with the issuance of a Form 483 containing five observations.

The company noted that the observations are addressable and fall within the scope of routine regulatory compliance. Dr. Reddy’s has stated that it is committed to responding to the USFDA within the prescribed timeline and implementing all necessary corrective and preventive actions to ensure full alignment with global quality standards.

In the meantime, Dr. Reddy’s Laboratories ended the session at ₹1,280, slightly above its opening price of ₹1,275. The stock touched an intraday high of ₹1,280.40 and a low of ₹1,267.30.