- Medical Devices
Recipient NameOmar S. Ishrak
Recipient TitleChief Executive Officer
- Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
710 Medtronic Parkway
Minneapolis, MN 55432
- Issuing Office:
- Office of Medical Device and Radiological Health Operations Division 2
- (407) 475-4700
Dear Mr. Ishrak:
The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter CMS # 560736. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.
Timothy G. Philips
Office of Medical Device and Radiological Health Operations (OMDRHO)
Division 2 – Central