This InspectorProfile is a report of relevant audit-related information on Andrew Garufi, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Medical Devices & Rad Health.
This InspectorProfile report is updated through and lists Andrew Garufi's 112 inspections in 12 countries: United States, Costa Rica, Canada, Italy, Israel, Switzerland, Germany, France, United Kingdom, Malta, Netherlands, and Austria.
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 Andrew Garufi'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 Andrew Garufi.
Note: The EIR and 483 documents are sold separately.Add To Cart36 of Andrew's 483s Available Now.