Jude Dike InspectorProfile

This FDA 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 Oct 2022 and lists Jude Dike's inspections in 14 countries: United States, China, Japan, Taiwan, France, United Kingdom, Belgium, Netherlands, Korea (the Republic of), Germany, Sweden, Denmark, Ireland, and Malaysia.

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.

Example Report

Below is an example of what a FDAzilla InspectorProfile report contains; This is not the actual data for Jude Dike.

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:
  • Company, site inspected, duration of inspection
  • Co-inspectors Karl Hezel, Eric Anderson, Cristina Dar, Cristina Ortega, Michael Nausin, year of last co-inspection, number of co-inspections
  • If a 483 issued, and whether or not it resulted in a warning letter.

Note: The EIR and 483 documents are sold separately.