This FDA InspectorProfile is a report of relevant audit-related information on Steven Kehoe, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Human Drugs.
This InspectorProfile report is updated through and lists Steven Kehoe's inspections in 23 countries: United States, India, Finland, United Kingdom, Germany, Ireland, Italy, South Africa, China, Switzerland, Spain, Canada, Sweden, Austria, Malta, France, Armenia, Hong Kong SAR, Taiwan, Portugal, Korea (the Republic of), United Arab Emirates, and Denmark.
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 Steven Kehoe'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 Steven Kehoe.
Note: The EIR and 483 documents are sold separately.