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USFDA completes pre-approval inspection at Dr. Reddy’s Visakhapatnam facility

15 Oct 2026 Evaluate

The United States Food and Drug Administration (USFDA) has completed a pre-approval inspection (PAI) at Dr. Reddy’s Laboratories’ FTO-9 manufacturing facility in Visakhapatnam, Andhra Pradesh. The inspection was conducted from October 8, 2026, to October 9, 2026. The company has been issued a Form 483 with three 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.

Peers
Company Name CMP
Sun Pharma. Inds. 1860.00
Dr. Reddys Labs. 1371.20
Cipla 1409.00
Lupin 1990.00
Zydus Lifesciences 1195.00
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