This FDA 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.
This InspectorProfile report is updated through and lists Suzie Kent's 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.
Note: The EIR and 483 documents are sold separately.