KNH

Kellia Hicks InspectorProfile

$995.00

This InspectorProfile is a report of relevant audit-related information on Kellia Hicks, 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 Kellia Hicks's 119 inspections in 14 countries: United States, Malaysia, Singapore, China, Ireland, United Kingdom, Germany, India, Netherlands, Canada, Belgium, Finland, Korea (the Republic of), and Spain.

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 Kellia Hicks'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 Kellia Hicks.

Example Report

Kellia Hicks FDA InspectorProfile Overview Example
Kellia Hicks FDA InspectorProfile Metrics Example
Kellia Hicks FDA InspectorProfile Citations Example
Kellia Hicks FDA InspectorProfile Inspections List
Add To Cart10 of Hicks 483s in stock

Product details

  • Kellia Hicks'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) Kellia Hicks has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart10 of Kellia's 483s Available Now.