This InspectorProfile is a report of relevant audit-related information on Seema Singh, 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 Seema Singh's 112 inspections in 12 countries: United States, Germany, Poland, Taiwan (Province of China), Taiwan, Japan, China, Korea (the Republic of), Italy, Spain, Canada, and Czech Republic.
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 Seema Singh'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 Seema Singh.
Note: The EIR and 483 documents are sold separately.Add To Cart22 of Seema's 483s Available Now.