This InspectorProfile is a report of relevant audit-related information on Rosanna Goodrich, 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 Rosanna Goodrich's 206 inspections in 17 countries: United States, Belgium, Germany, China, Indonesia, Italy, Czech Republic, Philippines, Taiwan, Hungary, Sweden, Finland, Spain, Denmark, France, United Kingdom, and Israel.
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 Rosanna Goodrich'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 Rosanna Goodrich.
Note: The EIR and 483 documents are sold separately.Add To Cart51 of Rosanna's 483s Available Now.