Home » FDA Hands Beckman Coulter 483 for CAPA, Process Validation Issues
FDA Hands Beckman Coulter 483 for CAPA, Process Validation Issues
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.
The GMP Letter
The GMP Letter
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