SECTOR
USFDA completes pre-approval inspection at Dr. Reddy’s FTO-11 facility in Andhra Pradesh
Oct-08-2026

The United States Food and Drug Administration (USFDA) has completed a Pre-Approval Inspection (PAI) at Dr. Reddy’s Laboratories’ FTO-11 manufacturing facility in Pydibhimavaram, Andhra Pradesh. The inspection was conducted from October 5, 2026 to October 7, 2026. The company has been issued a Form 483 with two observations.

Dr. Reddy's Laboratories is a multinational pharmaceutical company based in Hyderabad, Telangana in India. It manufactures and markets a wide range of pharmaceuticals in India and overseas.

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