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Aurobindo Pharma arm gets 'Voluntary Action Indicated' classification for Telengana facility from USFDA

Negative-35

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Aurobindo Pharma's subsidiary, Apitoria Pharma, received a Voluntary Action Indicated (VAI) classification from the US FDA. This follows an inspection of its Telangana API facility conducted between September 7 and 15, 2026. The classification indicates objectionable conditions were observed, requiring the company to voluntarily implement corrective measures.

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Read the original at Economic Times

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