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(25 Jun 2024, 12:12)

USFDA classifies inspection of Cipla's Patalganga unit as 'Voluntary Action Indicated'

Cipla announced that the United States Food and Drug Administration (USFDA) vide communication dated 25 June 2024 has classified the inspection of the company's manufacturing facility in Patalganga as Voluntary Action Indicated (VAI).

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