This InspectorProfile is a report of relevant audit-related information on Kirtida Patel, 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 Kirtida Patel's 172 inspections in 14 countries: United States, Mexico, Canada, India, France, Ireland, Germany, China, Taiwan, United Kingdom, Taiwan (Province of China), Japan, Australia, and Switzerland.
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 Kirtida Patel'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 Kirtida Patel.
Note: The EIR and 483 documents are sold separately.Add To Cart46 of Kirtida's 483s Available Now.