This InspectorProfile is a report of relevant audit-related information on Joshua Silvestri, 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 Joshua Silvestri's 220 inspections in 12 countries: Italy, France, United States, China, Germany, Canada, Korea (the Republic of), Belgium, Brazil, Mexico, Japan, and Taiwan.
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 Joshua Silvestri'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 Joshua Silvestri.
Note: The EIR and 483 documents are sold separately.
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