This FDA InspectorProfile is a report of relevant audit-related information on Sangeeta Khurana, 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 Sangeeta Khurana's inspections in 20 countries: India, United States, Italy, Sweden, Switzerland, Germany, China, France, Netherlands, United Kingdom, Canada, Japan, Denmark, Croatia, Korea (the Republic of), Czech Republic, Israel, Turkey, Greece, 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 Sangeeta Khurana'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 Sangeeta Khurana.
Note: The EIR and 483 documents are sold separately.