Laurus Labs announced that US Food and Drug Administration (USFDA) today completed a Pre-Approval Inspection (PAI) at its manufacturing facility at Unit-5, Parawada, Visakhapatnam, Andhra Pradesh. The inspection was conducted from 24 October 2022 to 28 October 2022. The company has been issued a Form 483 with one observation. The observation is procedural in nature. The Company will address the observation within stipulated timelines. Powered by Capital Market – Live News
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