Suzie Kent InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Suzie Kent, 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 Suzie Kent's 145 inspections in 8 countries: United States, Marshall Islands, Canada, United Kingdom, Italy, Spain, Korea (the Republic of), and Japan.

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 Suzie Kent'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 Suzie Kent.

Example Report

Suzie Kent FDA InspectorProfile Overview Example
Suzie Kent FDA InspectorProfile Metrics Example
Suzie Kent FDA InspectorProfile Citations Example
Suzie Kent FDA InspectorProfile Inspections List
Add To Cart5 of Kent 483s in stock

Product details

  • Suzie Kent'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) Suzie Kent has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart5 of Suzie's 483s Available Now.