This FDA InspectorProfile is a report of relevant audit-related information on Nancy Neiger, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Biologics.
This InspectorProfile report is updated through and lists Nancy Neiger's inspections in 12 countries: United States, Canada, Cuba, Korea (the Republic of), Austria, Denmark, Ireland, Germany, Romania, France, Sweden, and United Kingdom.
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 Nancy Neiger'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 Nancy Neiger.
Note: The EIR and 483 documents are sold separately.