Laurus Labs has informed 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 24th October 2022 to 28th October 2022. The company issued a Form 483 with one observation. The observation is procedural in nature. The Company will address the observation within stipulated timelines.
The above information is a part of company’s filings submitted to BSE.