Rebecca Davis InspectorProfile


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.

Product Description

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, Thailand, and France.

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.

Example Report

Rebecca Davis FDA InspectorProfile Overview Example
Rebecca Davis FDA InspectorProfile Metrics Example
Rebecca Davis FDA InspectorProfile Citations Example
Rebecca Davis FDA InspectorProfile Inspections List
Add To Cart17 of Davis 483s in stock

Product details

  • Rebecca Davis's metrics:
    • 483 issue rate, total inspections, total 483s
    • Most common citations (based on CFR), CFR description, and citation frequency
    • Total inspections, total 483s
    • Longest / shortest inspection in duration - all time, last year
    • Total warning letters
  • Inspection details for each inspection (since 2000) Rebecca Davis has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart17 of Rebecca's 483s Available Now.