This FDA InspectorProfile is a report of relevant audit-related information on Francis Guidry, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Foods & Cosmetics.
This InspectorProfile report is updated through and lists Francis Guidry's inspections in 23 countries: United States, Ireland, United Kingdom, Sweden, Denmark, Switzerland, Spain, Canada, France, Italy, Germany, Finland, Hungary, China, Japan, Taiwan, Thailand, Mexico, South Africa, Korea (the Republic of), Netherlands, India, and New Zealand.
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 Francis Guidry'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 Francis Guidry.
Note: The EIR and 483 documents are sold separately.