Ajanta Pharma Paithan facility gets VAI from US FDA
AJANTPHARM · price
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Ajanta Pharma received the Establishment Inspection Report from the US FDA for its Paithan, Maharashtra manufacturing facility. The inspection has been classified as Voluntary Action Indicated (VAI), meaning the facility is in acceptable condition with no mandatory corrective action required. The cGMP inspection was conducted from 13 April to 21 April 2026.
Positive outcome — VAI means no FDA action needed, supports continued US exports from Paithan and removes near-term compliance uncertainty.