Dr. Reddy's Laboratories Ltd. - Form 6-K Filing

Dr. Reddy's Laboratories Limited has filed a Form 6-K report detailing a recent inspection by the United States Food and Drug Administration (USFDA). The inspection, a Pre-Approval Inspection (PAI), took place at their FTO-11 manufacturing facility in Pydibhimavaram, Andhra Pradesh, from October 5-7, 2026. The company received a Form 483 with two observations, which they plan to address within the specified timeframe. This filing is made in accordance with Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015.