The United States Food and Drug Administration (USFDA) have conducted GMP inspection at Indoco Remedies’ Solid Oral Formulation Facility (Plant 1) in Goa. The inspection was conducted from January 16, 2023 to January 20, 2023.
The USFDA has issued Form 483 with 9 observations, which will be addressed within stipulated time. The company is committed to maintain compliances across all our facilities with cGMP quality standards at all times.
Indoco Remedies is engaged in the manufacturing and marketing of formulations (finished dosage forms) and active pharmaceutical ingredients (APIs) in India.