This InspectorProfile is a report of relevant audit-related information on Rebecca Davis, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Biologics.
This InspectorProfile report is updated through and lists Rebecca Davis's 388 inspections in 19 countries: United States, Lithuania, Estonia, Latvia, Korea (the Republic of), India, Malaysia, Philippines, Dominican Republic, Dominican Republic (the), Japan, China, Germany, Romania, Denmark, Ukraine, Poland, France, and Thailand.
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 Rebecca Davis'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 Rebecca Davis.
Note: The EIR and 483 documents are sold separately.Add To Cart16 of Rebecca's 483s Available Now.