Linda Murphy InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Linda Murphy, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Human Drugs.

Product Description

This InspectorProfile report is updated through and lists Linda Murphy's 103 inspections in 16 countries: United States , India , Belgium , Hong Kong SAR , Switzerland , Italy , Macao , Singapore , Thailand , Austria , Malaysia , Taiwan , Korea (the Republic of) , France , Canada , and Japan .

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 Linda Murphy'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 Linda Murphy.

Example Report

Linda Murphy FDA InspectorProfile Overview Example
Linda Murphy FDA InspectorProfile Metrics Example
Linda Murphy FDA InspectorProfile Citations Example
Linda Murphy FDA InspectorProfile Inspections List
Add To Cart55 of Murphy 483s in stock

Product details

  • Linda Murphy'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) Linda Murphy has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart55 of Linda's 483s Available Now.