Kathleen Tormey InspectorProfile


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

Product Description

This InspectorProfile report is updated through and lists Kathleen Tormey's 172 inspections in 10 countries: United States, Latvia, Canada, Poland, China, Germany, Austria, Italy, Switzerland, and Denmark.

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 Kathleen Tormey'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 Kathleen Tormey.

Example Report

Kathleen Tormey FDA InspectorProfile Overview Example
Kathleen Tormey FDA InspectorProfile Metrics Example
Kathleen Tormey FDA InspectorProfile Citations Example
Kathleen Tormey FDA InspectorProfile Inspections List
Add To Cart29 of Tormey 483s in stock

Product details

  • Kathleen Tormey'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) Kathleen Tormey has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart29 of Kathleen's 483s Available Now.