Kelvin Cheung InspectorProfile


This InspectorProfile is a report of relevant audit-related information on Kelvin Cheung, 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 Kelvin Cheung's 377 inspections in 17 countries: United States, Germany, Switzerland, Ireland, France, Taiwan, Japan, China, Malaysia, Israel, Korea (the Republic of), Spain, Italy, Korea, Republic Of (South), Singapore, Denmark, and Netherlands.

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 Kelvin Cheung'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 Kelvin Cheung.

Example Report

Kelvin Cheung FDA InspectorProfile Overview Example
Kelvin Cheung FDA InspectorProfile Metrics Example
Kelvin Cheung FDA InspectorProfile Citations Example
Kelvin Cheung FDA InspectorProfile Inspections List
Add To Cart77 of Cheung 483s in stock

Product details

  • Kelvin Cheung'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) Kelvin Cheung has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart77 of Kelvin's 483s Available Now.