Lisa Orr InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Lisa Orr, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Human Drugs.

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 Lisa Orr'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 Lisa Orr.

Example Report

Lisa Orr FDA InspectorProfile Overview Example
Lisa Orr FDA InspectorProfile Metrics Example
Lisa Orr FDA InspectorProfile Citations Example
Lisa Orr FDA InspectorProfile Inspections List
Add To CartLisa Orr 483s

Product details

  • Lisa Orr'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) Lisa Orr has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To CartLisa Orr 483s