Manufacturing FDA dings Piramal API plant with Form 483 detailing problems tied to quality control, equipment cleaning and more By Fraiser Kansteiner Feb 26, 2025 10:22am Piramal U.S. FDA Form 483 ...

Despite receiving a prior wrist slap from the FDA in the shape of a Form 483, Sanofi is still working to right the ship at a U.S. | The FDA has slapped a warning letter on Sanofi’s Genzyme ...