Teresa Kastner InspectorProfile


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.

Product Description

This InspectorProfile report is updated through and lists Teresa Kastner's 136 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.

Example Report

Teresa Kastner FDA InspectorProfile Overview Example
Teresa Kastner FDA InspectorProfile Metrics Example
Teresa Kastner FDA InspectorProfile Citations Example
Teresa Kastner FDA InspectorProfile Inspections List
Add To Cart28 of Kastner 483s in stock

Product details

  • Teresa Kastner's metrics:
    • 483 issue rate, total inspections, total 483s
    • Most common citations (based on CFR), CFR description, and citation frequency
    • Total inspections, total 483s
    • Longest / shortest inspection in duration - all time, last year
    • Total warning letters
  • Inspection details for each inspection (since 2000) Teresa Kastner has conducted including:

Note: The EIR and 483 documents are sold separately.

Add To Cart28 of Teresa's 483s Available Now.