This InspectorProfile is a report of relevant audit-related information on Vickie Kanion, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Biologics.
This InspectorProfile report is updated through and lists Vickie Kanion's 138 inspections in 10 countries: United States, Canada, China, Taiwan, Belgium, Germany, France, India, Italy, and Poland.
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 Vickie Kanion'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 Vickie Kanion.
Note: The EIR and 483 documents are sold separately.Add To Cart8 of Vickie's 483s Available Now.