This InspectorProfile is a report of relevant audit-related information on Jacqueline 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 Jacqueline Warner's 337 inspections in 22 countries: United States , Italy , Germany , Denmark , Ireland , Switzerland , Austria , France , United Kingdom , Norway , Sweden , China , Brazil , Canada , Spain , Taiwan , India , Finland , Korea (the Republic of) , Japan , Belgium , 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 Jacqueline 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 Jacqueline Warner.
Note: The EIR and 483 documents are sold separately.Add To Cart48 of Jacqueline's 483s Available Now.