Dr. Reddys Laboratories Ltd.

United States Food & Drug Administration (USFDA) has completed a Pre-Approval Inspection (PAI) and a routine GMP inspection at Dr. Reddy's Laboratories’ API manufacturing facility in Srikakulam, Andhra Pradesh, India (CTO-6). The inspection was conducted from July 10, 2023 to July 19, 2023. The inspection closed with zero observations and a classification of No Action Indicated (NAI). 

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.