Matthew R Noonan
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Detailed Analysis
Matthew R Noonan meticulously examines each stage of manufacturing processes, focusing on adherence to regulations, product quality, and consumer safety. He places significant emphasis on the effectiveness of corrective actions, process validation, cleanliness, and control over material handling.
Matthew R Noonan is a detail-oriented FDA investigator who prioritizes compliance with manufacturing processes, contamination control, and product quality assurance. He focuses on identifying deficiencies in key areas such as complaint management, corrective and preventive actions, batch manufacturing, process validation, cleaning validation, labeling control, sample testing, preventive maintenance, and material receipt & inspection.
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