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Company Statement

Biocon's Generic Formulations Facility in Bengaluru completes U.S. FDA Inspection with No 483 observations

Bengaluru, India, November 12, 2018

"This is to inform you that the U.S. FDA conducted a pre approval inspection of our new Oral Solid Dosage Forms manufacturing facility at Biocon Park/ Bengaluru/ from Nov 05- Nov 09/ 2018. The audit concluded without any observations and no Form 483 was issued. The successful audit of this site reflects our strong commitment to quality and cGMP compliance. N
-Company Spokesperson


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