Aurobindo Pharma announced that the United States Food and Drug Administration (US FDA) conducted its pre-approval inspection (PAI) and GMP inspection from 22 August to 26 August 2022, of Unit at Raleigh, North Carolina, USA, (owned by Aurolife Pharma LLC, a wholly owned subsidiary of the company) established for manufacturing MDI (Metered Dose Inhalers) and Derma products. The Unit has filed 2 Derma products and 1 MDI product. At the end of the inspection, Aurolife has been issued a Form 483 with 1 observation and the observation is procedural in nature and there are no data integrity issues. Powered by Capital Market – Live News
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