This FDA InspectorProfile is a report of relevant audit-related information on Keegan Mixon, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Foods & Cosmetics.
This InspectorProfile report is updated through and lists Keegan Mixon's inspections in 2 countries: United States, and Canada.
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 Keegan Mixon'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 Keegan Mixon.
Note: The EIR and 483 documents are sold separately.