Andrew Garufi
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Detailed Analysis
Auditor Garufi tends to focus and place high priority on the adherence to the basis of Medical Device Reporting, ensuring not only is reporting done, but is done in a timely manner. He methodically examines the presence and implementation of written MDR procedures.
Andrew Garufi is an FDA auditor with a keen eye for Medical Device Reporting (MDR) compliance. He has demonstrated a strong interest in institutional adherence to required reporting protocols, under FDA Form 3500A, for device-related patient deaths. He emphasizes on the necessity of written MDR procedures and timeliness of reporting. Garufi is particularly watchful of healthcare institutions' response to device-associated infections, possibly pointing towards a preference for comprehensive patient safety measures.
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