RMG

Rosanna Goodrich InspectorProfile

$795

This InspectorProfile is a report of relevant audit-related information on Rosanna Goodrich, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Medical Devices & Rad Health.

This report is updated through .

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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 Rosanna Goodrich'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 Rosanna Goodrich.

Example Report

Rosanna Goodrich FDA InspectorProfile Overview Example
Rosanna Goodrich FDA InspectorProfile Metrics Example
Rosanna Goodrich FDA InspectorProfile Citations Example
Rosanna Goodrich FDA InspectorProfile Inspections List
Add To CartRosanna Goodrich 483s

Product details

  • Rosanna Goodrich'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) Rosanna Goodrich has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To CartRosanna Goodrich 483s