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USFDA issues Form 483 with five inspectional observations to Marksans Pharma#39;s Goa unit

USFDA issues Form 483 with five inspectional observations to Marksans Pharma#39;s Goa unit The US Food and Drug Administration (USFDA) had conducted a routine current Good Manufacturing Practices (cGMP) inspection at the manufacturing facility from April 9-17, 2024, the company said in a regulatory filing.

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