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Dr. Reddy's Laboratories Receives Form 483 from USFDA After API Manufacturing Facility Inspection

June 7, 2024, 6:55 p.m.
  • United States Food & Drug Administration (USFDA) completes GMP inspection at Dr. Reddy's API manufacturing facility in Srikakulam, Andhra Pradesh.
  • Inspection conducted from May 30…

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