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Home » Hospira Device Plant Receives Form 483 for Infusion Pump Battery Failures
Hospira Device Plant Receives Form 483 for Infusion Pump Battery Failures
Hospira’s Lake Forest, Ill., manufacturing facility received an FDA Form 483 for numerous quality system deviations related to its infusion pumps, including inadequate design validation, inadequate design change procedures and inadequate corrective and preventive action procedures.