NOTIFICATION TO STOCK EXCHANGE
COMPANY STATEMENT
This is to inform that the U.S. Food and Drug Administration (US FDA) conducted a GMP surveillance inspection of our API facility (Site 6), located at Visakhapatnam, Andhra Pradesh, between 3rd and 7th November, 2025.
Two observations were cited at the end of the inspection, which the Company will be addressing within the stipulated time. The Company does not foresee any impact on the business.
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You are now leaving the Biocon website for a Biocon affiliate site or third party site that is solely responsible for its content, including its compliance with guidelines applicable in certain geographies. Links to Biocon affiliate sites and third party sites are provided as a resource to our visitors and may not be governed by the same regulatory requirements applicable to this site and unaffiliated third party sites are subject to their own terms and data protection notices and practices. Moreover, if their third party site is subject to other country laws, regulatory requirements, data protection requirements or medical practices may differ between countries and the information provided therein may not be suitable for use in your country.
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