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 221 inspections in 17 countries: United States, Spain, Germany, France, Ireland, Australia, Korea (the Republic of), China, Italy, Canada, Japan, Singapore, Israel, Costa Rica, Switzerland, Malaysia, and Denmark.
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 Cart67 of Lisa's 483s Available Now.