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Matthew Vernon InspectorProfile

$795

This InspectorProfile is a report of relevant audit-related information on Matthew Vernon, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Medical Devices & Rad Health.

This report is updated through .

FDA audits are stressful. Whether you are issued a 483 depends largely on your compliance with GxP and predicate rules; but it can also depend on the Agency's current focus and the tendencies of your specific investigator(s). FDAzilla has curated Matthew Vernon's inspection information so that you can mitigate investigator-related risks.

Below is an example of what a FDAzilla InspectorProfile report contains; This is not the actual data for Matthew Vernon.

Example Report

Matthew Vernon FDA InspectorProfile Overview Example
Matthew Vernon FDA InspectorProfile Metrics Example
Matthew Vernon FDA InspectorProfile Citations Example
Matthew Vernon FDA InspectorProfile Inspections List
Add To CartMatthew Vernon 483s

Product details

  • Matthew Vernon's metrics:
    • 483 issue rate, total inspections, total 483s
    • Most common citations (based on CFR), CFR description, and citation frequency
    • Total inspections, total 483s
    • Longest / shortest inspection in duration - all time, last year
    • Total warning letters
  • Inspection details for each inspection (since 2000) Matthew Vernon has conducted including:
    • Company, site inspected, duration of inspection
    • Co-inspectors , year of last co-inspection, number of co-inspections
    • If a 483 issued, and whether or not it resulted in a warning letter.

Note: The EIR and 483 documents are sold separately.

Add To CartMatthew Vernon 483s