[ad_1] Dr Reddy’s Laboratories Ltd on Friday, September 6, announced that it has received an Establishment Inspection Report (EIR) from the United States Food & Drug Administration (USFDA) for its manufacturing facility (CTO-6) in Srikakulam, Andhra Pradesh. The inspection has been classified as “Voluntary Action Indicated” (VAI) by the US drug regulator, meaning that while some […]