This InspectorProfile is a report of relevant audit-related information on Sean Creighton, 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 Sean Creighton's 300 inspections in 31 countries: United States, India, Taiwan, Israel, Ireland, Germany, China, United Kingdom, Hungary, Costa Rica, Japan, Malaysia, Denmark, Switzerland, Austria, Poland, Romania, Serbia, Dominican Republic (the), Sweden, Singapore, South Africa, Korea (the Republic of), Belgium, Taiwan (Province of China), Netherlands, Czech Republic, Estonia, France, Finland, and Hong Kong SAR.
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 Sean Creighton'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 Sean Creighton.
Note: The EIR and 483 documents are sold separately.Add To Cart35 of Sean's 483s Available Now.