Wendy Blame InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Wendy Blame, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Medical Devices & Rad Health.

Product Description

This InspectorProfile report is updated through and lists Wendy Blame's 215 inspections in 11 countries: United States, Dominican Republic (the), Mexico, China, Canada, France, Belgium, United Kingdom, Italy, Sweden, and Peru.

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 Wendy Blame'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 Wendy Blame.

Example Report

Wendy Blame FDA InspectorProfile Overview Example
Wendy Blame FDA InspectorProfile Metrics Example
Wendy Blame FDA InspectorProfile Citations Example
Wendy Blame FDA InspectorProfile Inspections List
Add To Cart31 of Blame 483s in stock

Product details

  • Wendy Blame'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) Wendy Blame has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart31 of Wendy's 483s Available Now.