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Sanofi unit in Ireland chided by FDA over manufacturing flubs linked to Altuviiio

1st July 2026 Uncategorised 0

After a site visit by FDA inspectors yielded a Form 483 for Genzyme Ireland in early 2026, the Sanofi subsidiary is facing further reprimand from the U.S. regulator.

More: Sanofi unit in Ireland chided by FDA over manufacturing flubs linked to Altuviiio
Source: fierce

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Sanofi unit in Ireland chided by FDA over manufacturing flubs linked to Altuviiio

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