The United States Food and Drug Administration (USFDA) has concluded inspection at Aurobindo Pharma’s step-down subsidiary – Eugia SEZ’s injectable facility situated at Polepally Village, Telangana.
USFDA had conducted an inspection from February 19 to 29, 2024. The inspection closed with 7 observations. The observations are procedural in nature and will be responded to within the stipulated time.
Aurobindo Pharma is engaged in manufacturing pharmaceutical products. It offers active pharmaceutical ingredients, intermediates and generic formulations like astemizole, domeperidone and omeprazole; anti-infective, oral and sterile antibiotics, pain management and osteoporosis segments.
