We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » FDA Hands Beckman Coulter 483 for CAPA, Process Validation Issues
FDA Hands Beckman Coulter 483 for CAPA, Process Validation Issues
July 7, 2011
Device giant Beckman Coulter has been handed a Form 483 for observations related to corrective and preventive action (CAPA) procedures, process validation, incoming product acceptance procedures and device design validation.