Kathy Kuo InspectorProfile


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

Product Description

This InspectorProfile report is updated through and lists Kathy Kuo's 3 inspections in 1 countries: and United States.

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 Kathy Kuo'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 Kathy Kuo.

Example Report

Kathy Kuo FDA InspectorProfile Overview Example
Kathy Kuo FDA InspectorProfile Metrics Example
Kathy Kuo FDA InspectorProfile Citations Example
Kathy Kuo FDA InspectorProfile Inspections List
Add To Cart2 of Kuo 483s in stock

Product details

  • Kathy Kuo'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) Kathy Kuo has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart2 of Kathy's 483s Available Now.