The United States Food and Drug Administration (USFDA) has concluded an inspection at Lupin’s manufacturing facility located in Goa, India. The inspection was conducted from October 19, 2026, to October 23, 2026, and closed with the issuance of a Form-483 with one observation.
The company will address the observation and respond to the USFDA within the stipulated timeframe. It is committed to be compliant with CGMP standards across all its facilities.
Lupin is an innovation led transnational pharmaceutical company producing, developing and marketing a wide range of branded and generic formulations, biotechnology products and active pharmaceutical ingredients (APIs) globally.