Dr. Reddys Laboratories Ltd.

United States Food & Drug Administration (USFDA) has completed a GMP inspection at Dr. Reddy's Laboratories’ API manufacturing facility (CTO-6) in Srikakulam, Andhra Pradesh. The inspection was conducted from May 30, 2024 to June 7, 2024. The company has been issued a Form 483 with four observations, which it will address within the stipulated timeline. 

Dr. Reddy's Laboratories is a multinational pharmaceutical company based in Hyderabad, Telangana in India. It manufactures and markets a wide range of pharmaceuticals in India and overseas.