defencath — CRL

“On August 8, 2022, CorMedix Inc. (the "Company") issued a press release announcing that a second Complete Response Letter was received from the U.S. Food and Drug Administration ("FDA"), stating that the New Drug Application ("NDA") for DefenCath cannot be approved until the deficiencies conveyed to the contract manufacturing organization and the supplier of the active pharmaceutical ingredient heparin during inspections are resolved to the satisfaction of FDA.”