This InspectorProfile is a report of relevant audit-related information on Thomas Peter, 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 Thomas Peter's 75 inspections in 14 countries: United States, Sweden, Switzerland, France, Belgium, Italy, Germany, China, Japan, United Kingdom, Malaysia, Brazil, Canada, and Taiwan.
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 Thomas Peter'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 Thomas Peter.
Note: The EIR and 483 documents are sold separately.Add To Cart18 of Thomas's 483s Available Now.