Dr Reddy's receives two USFDA observations for New York API...

Dr Reddy's receives two USFDA observations for New York API facility

Сообщение

Dr. Reddy's Laboratories faced USFDA scrutiny at its New York API facility, receiving a Form 483 with two observations after a GMP inspection concluded on May 16, 2025. The company will address these concerns within the given timeframe.

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