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Cipla Subsidiary Keeps VAI Status After USFDA Unit 3 Inspection

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Sig2.13Sen+0.17Env0.00Soc0.00Gov-1.00

InvaGen Pharmaceuticals’ Unit 3 in Central Islip underwent a routine USFDA cGMP inspection from July 13 to July 17, 2026, ending with one inspectional observation on Form 483. The facility maintained its Voluntary Action Indicated status, with the observation addressed and no Warning Letter or Import Alert triggered. The VAI classification supports uninterrupted US generic manufacturing and supply.

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