Dr. Reddy’s Srikakulam plant gets VAI tag from U.S. FDA
[ad_1] Generic drugmaker Dr. Reddy’s Laboratories has received establishment inspection report (EIR) for its Srikakulam formulations manufacturing facility from the U.S. Food and Drug Administration (U.S. FDA) with a voluntary action indicated (VAI) classification. Following a good manufacturing practice (GMP) and a pre-approval inspection (PAI) in July, the facility (FTO 11) received seven observations from […]
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