This InspectorProfile is a report of relevant audit-related information on Teresa Kastner, 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 Teresa Kastner's 130 inspections in 11 countries: United States, China, Japan, Canada, Belgium, Iceland, Germany, Poland, France, United Kingdom, and Italy.
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 Teresa Kastner'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 Teresa Kastner.
Note: The EIR and 483 documents are sold separately.Add To Cart22 of Teresa's 483s Available Now.