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Dr Reddy's Lab gets EIR from USFDA for Srikakulam facility
Dr Reddy’s Laboratories has received an Establishment Inspection Report (EIR) from the USFDA for its Srikakulam formulations manufacturing facility. The inspection outcome was classified as Voluntary Action Indicated (VAI), officially closing the inspection. This inspection included both a Good Manufacturing Practice (GMP) review and a Pre-Approval Inspection (PAI).