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Home » FDA Raps Devon Orthopaedic Implants for Improper Complaint Handling, Event Reporting
FDA Raps Devon Orthopaedic Implants for Improper Complaint Handling, Event Reporting
Devon Orthopaedic Implants received a Form 483 from the FDA following a May inspection of its facility in King of Prussia, Pa., for failing to fully investigate complaints or report possible medical device issues.