Leighton Ngai InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Leighton Ngai, 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 Leighton Ngai's 223 inspections in 10 countries: United States, United Kingdom, Switzerland, Taiwan, China, Ireland, Japan, Malaysia, Korea (the Republic of), and Poland.

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 Leighton Ngai'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 Leighton Ngai.

Example Report

Leighton Ngai FDA InspectorProfile Overview Example
Leighton Ngai FDA InspectorProfile Metrics Example
Leighton Ngai FDA InspectorProfile Citations Example
Leighton Ngai FDA InspectorProfile Inspections List
Add To Cart44 of Ngai 483s in stock

Product details

  • Leighton Ngai'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) Leighton Ngai has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart44 of Leighton's 483s Available Now.