USFDA concludes inspection of Time-Cap Laboratories' manufacturing facility in New York

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On conclusion of the inspection, the Subsidiary has received One (1) inspectional observation in Form 483. There is no data integrity observation. The Subsidiary will work closely with the USFDA and is committed to address the observation comprehensively within the stipulated time.
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First Published: Apr 28 2025 | 12:58 PM IST