“The company will respond to the FDA with an appropriate Corrective and Preventive Action Plan (CAPA) and are confident of addressing these observations expeditiously. The FDA has set a target action date for our insulin Glargine application in June 2020. We believe the outcome of this inspection does not, in any way, impact the commercialization plans of insulin Glargine in the US. Biocon Biologics is committed to global standards of quality and compliance,” Biocon’s spokesperson said.
As per the US FDA, Form 483 is issued to firm management at the conclusion of an inspection when investigators observe any conditions that, in their judgment, may constitute violations of the Food Drug and Cosmetic Act and related Acts.