Matthew Humbard InspectorProfile

$795

This InspectorProfile is a report of relevant audit-related information on Matthew Humbard, 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 Nov 22 2019 and lists Matthew Humbard's 2 inspections in 2 countries: Canada, and Austria.

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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 Matthew Humbard'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 Matthew Humbard.

Example Report

Matthew Humbard FDA InspectorProfile Overview Example

Matthew Humbard FDA InspectorProfile Metrics Example

Matthew Humbard FDA InspectorProfile Citations Example

Matthew Humbard FDA InspectorProfile Inspections List

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Product details

Matthew Humbard'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) Matthew Humbard has conducted including:
- Company, site inspected, duration of inspection
- Co-inspectors like Laureen Geniusz FDA, 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.

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