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Aurobindo Pharma receives OAI from USFDA for oral solids manufacturing facility

30 Jan 2020 Evaluate

Aurobindo Pharma has received a letter from US Food and Drug Administration (USFDA) classifying the inspection conducted at Unit VII, an oral solids formulation manufacturing facility as Official Action Indicated (OAI). The inspection was conducted on October 7 to 11, 2019.

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.

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