GML

Geoffrey Leist InspectorProfile

$695

This InspectorProfile is a report of relevant audit-related information on Geoffrey Leist, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Foods & Cosmetics.

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 Geoffrey Leist'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 Geoffrey Leist.

Example Report

Geoffrey Leist FDA InspectorProfile Overview Example
Geoffrey Leist FDA InspectorProfile Metrics Example
Geoffrey Leist FDA InspectorProfile Citations Example
Geoffrey Leist FDA InspectorProfile Inspections List
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Product details

  • Geoffrey Leist'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) Geoffrey Leist 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.

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