MEP

Mark Parmon InspectorProfile

$995

This InspectorProfile is a report of relevant audit-related information on Mark Parmon, 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 Mark Parmon's 243 inspections in 8 countries: United States, United Kingdom, Italy, Canada, Ireland, France, Portugal, and Denmark.

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 Mark Parmon'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 Mark Parmon.

Example Report

Mark Parmon FDA InspectorProfile Overview Example
Mark Parmon FDA InspectorProfile Metrics Example
Mark Parmon FDA InspectorProfile Citations Example
Mark Parmon FDA InspectorProfile Inspections List
Add To Cart18 of Parmon 483s in stock

Product details

  • Mark Parmon'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) Mark Parmon has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart18 of Mark's 483s Available Now.