This FDA InspectorProfile is a report of relevant audit-related information on Terry Kimball, 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 Terry Kimball's inspections in 11 countries: United States, Germany, United Kingdom, Denmark, Italy, Ireland, India, China, Austria, Switzerland, and Korea, Republic Of (South).
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 Terry Kimball'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 Terry Kimball.
Note: The EIR and 483 documents are sold separately.