This FDA InspectorProfile is a report of relevant audit-related information on Noreen Muniz, a U.S. Food & Drug Administration investigator who primarily conducts inspections in the area of Human Drugs.
This InspectorProfile report is updated through and lists Noreen Muniz's inspections in 16 countries: United States, China, Canada, France, Taiwan, Korea, Republic Of (South), United Kingdom, Mexico, Italy, Argentina, Spain, Germany, Switzerland, Belgium, Israel, and Japan.
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 Noreen Muniz'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 Noreen Muniz.
Note: The EIR and 483 documents are sold separately.