CLR

Clifton Randell InspectorProfile

$795

This InspectorProfile is a report of relevant audit-related information on Clifton Randell, 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 Clifton Randell's 3 inspections in 1 countries: and United States.

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 Clifton Randell'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 Clifton Randell.

Example Report

Clifton Randell FDA InspectorProfile Overview Example
Clifton Randell FDA InspectorProfile Metrics Example
Clifton Randell FDA InspectorProfile Citations Example
Clifton Randell FDA InspectorProfile Inspections List
Add To Cart1 of Randell 483s in stock

Product details

  • Clifton Randell'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) Clifton Randell has conducted including:
    • Company, site inspected, duration of inspection
    • Co-inspectors , 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 Cart1 of Clifton's 483s Available Now.