Thilak Mudalige InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Thilak Mudalige, 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 Thilak Mudalige's 1 inspections in 1 countries: and Ireland.

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 Thilak Mudalige'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 Thilak Mudalige.

Example Report

Thilak Mudalige FDA InspectorProfile Overview Example
Thilak Mudalige FDA InspectorProfile Metrics Example
Thilak Mudalige FDA InspectorProfile Citations Example
Thilak Mudalige FDA InspectorProfile Inspections List
Add To Cart

Product details

  • Thilak Mudalige'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) Thilak Mudalige has conducted including:
    • Company, site inspected, duration of inspection
    • Co-inspectors like Leighton Ngai FDA, year of last co-inspection, number of co-inspections
    • If a 483 issued, and whether or not it resulted in a warning letter.

Note: The EIR and 483 documents are sold separately.

Add To Cart