Jude Dike InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Jude Dike, 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 Jude Dike's 99 inspections in 11 countries: United States, China, Japan, Taiwan (Province of China), Taiwan, France, United Kingdom, Belgium, Netherlands, Ireland, 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 Jude Dike'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 Jude Dike.

Example Report

Jude Dike FDA InspectorProfile Overview Example
Jude Dike FDA InspectorProfile Metrics Example
Jude Dike FDA InspectorProfile Citations Example
Jude Dike FDA InspectorProfile Inspections List
Add To Cart18 of Dike 483s in stock

Product details

  • Jude Dike'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) Jude Dike has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart18 of Jude's 483s Available Now.