Bonnie Conley InspectorProfile


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

This report is updated through .

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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 Bonnie Conley's inspection information so that you can mitigate investigator-related risks.

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  • Bonnie Conley'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) Bonnie Conley has conducted including:
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