This FDA InspectorProfile is a report of relevant audit-related information on Diane Van Leeuwen, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Human Drugs.
This InspectorProfile report is updated through and lists Diane Van Leeuwen's inspections in 14 countries: United States, Canada, France, Germany, Netherlands, Switzerland, Russia, Japan, United Kingdom, Australia, Denmark, Greece, Portugal, and Indonesia.
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 Diane Van Leeuwen'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 Diane Van Leeuwen.
Note: The EIR and 483 documents are sold separately.