Cipla gets 6 observations from USFDA for Goa facility
Drug Approval

Cipla gets 6 observations from USFDA for Goa facility

The company will work closely with the USFDA and is committed to address these comprehensively within stipulated time

  • By IPP Bureau | June 24, 2024

USFDA has conducted an inspection at the Cipla Ltd's manufacturing facility in Goa, India from 10th - 21st June 2024.

On conclusion of the inspection, the company received 6 (six) inspectional observations in Form 483. The company will work closely with the USFDA and is committed to address these comprehensively within stipulated time.

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