This InspectorProfile is a report of relevant audit-related information on Lisa Warner, 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 Lisa Warner's 196 inspections in 16 countries: United States, Spain, Germany, France, Ireland, Australia, Korea (the Republic of), China, Italy, Canada, Japan, Singapore, Israel, Costa Rica, Switzerland, and Malaysia.
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 Lisa Warner'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 Lisa Warner.
Note: The EIR and 483 documents are sold separately.Add To Cart33 of Lisa's 483s Available Now.