Dr. Reddy's Laboratories Limited announced that the United States Food & Drug Administration (USFDA) completed a GMP inspection at its API manufacturing facility (CTO-5) in Miryalaguda, Telangana, India. The inspection was conducted from 19 May 2025 to 24 May 2025. The company has been issued a Form 483 with 2 observations, which it will address within the stipulated timeline.