Zydus injectable facility in Vadodara gets U.S. FDA inspection report with VAI status
The U.S. Food and Drug Administration has issued an establishment inspection report (EIR) with a voluntary action indicated (VAI) classification to an injectable facility of Zydus Lifesciences in Vadodara. The company received the EIR for a GMP follow-up inspection the U.S. FDA conducted at the facility in Jarod, Vadodara, from August 25 to September 5, […]
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