Benjamin J Smith
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Detailed Analysis
Benjamin J Smith takes an exhaustive approach towards identifying any potential issues, with a major focus on device controls, complaint addressing efficiency, and MDR reporting. He prioritizes proper documentation and completeness of protocols.
FDA auditor Benjamin J Smith is focused on compliance with MDR report timelines and effectiveness of procedures for device control and distribution. He exhibits a keen interest in following up on device specification failures and manages to identify procedural loopholes related to complaint handling systems. He's thorough in his approach, with an emphasis on proper and complete documentation.
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