This FDA InspectorProfile is a report of relevant audit-related information on Brian Keefer, 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 Brian Keefer's inspections in 17 countries: Italy, Germany, United States, Denmark, United Kingdom, Switzerland, Sweden, Austria, Japan, Russia, Netherlands, France, Hungary, Mexico, Slovenia, Canada, and Ireland.
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 Brian Keefer'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 Brian Keefer.
Note: The EIR and 483 documents are sold separately.