USFDA concludes inspection at Cipla’s manufacturing facility in Bengaluru

14 Nov 2024 Evaluate

The United States Food and Drug Administration (USFDA) has concluded the inspection at Cipla’s manufacturing facility in Virgonagar, Bengaluru. The inspection was conducted from 7th - 13th November 2024.

On conclusion of the inspection, the Company received 8 observations in Form 483. The Company will work closely with the USFDA and remains committed to address these observations comprehensively within stipulated time.

Cipla is a global pharmaceutical company which uses cutting edge technology and innovation to meet the everyday needs of all patients.

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