This InspectorProfile is a report of relevant audit-related information on Elizabeth Griffin, 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 Elizabeth Griffin's 219 inspections in 13 countries: United States, Germany, Switzerland, France, Ireland, United Kingdom, Sweden, Canada, Italy, Netherlands, China, Taiwan (Province of China), and Costa Rica.
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 Elizabeth Griffin'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 Elizabeth Griffin.
Note: The EIR and 483 documents are sold separately.Add To Cart25 of Elizabeth's 483s Available Now.