Mumbai, April 17 -- Cipla announced that that the USFDA has conducted an inspection at the Company's manufacturing facility in Verna, Goa from 6 to 17 April 2026. The inspection was a routine current Good Manufacturing Practices (cGMP) inspection and a Pre-Approval Inspection (PAI). On conclusion of the inspection, the Company received two (2) inspectional observations in Form 483.

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