FDA 483 - Cameron G. Javid, M.D. - February 16, 2023

An FDA inspection of Cameron G. Javid, M.D., a clinical investigator in Tucson, AZ, revealed a significant deficiency in maintaining adequate and accurate case histories. Specifically, adverse events and concomitant medications noted in source documents were either inactivated or not included in electronic case report forms for a reviewed protocol. This indicates a failure to ensure complete and accurate data pertinent to the investigation.