CLOSEOUT LETTER
Beckman Coulter, Inc. MARCS-CMS 678042 —
- Delivery Method:
- VIA Electronic Mail
- Product:
- Medical Devices
- Recipient:
-
Recipient NameKevin O’Reilly
-
Recipient TitlePresident
- Beckman Coulter, Inc.
- Beckman Coulter Diagnostics
1000 Lake Hazeltine Drive
Chaska, MN 55318-1037
United States-
- Koreilly@DHDiagnostics.com
- Issuing Office:
- Division of Medical Device and Radiological Health Operations Central
United States
United States
Dear Mr. O’Reilly:
The Food and Drug Administration has completed an evaluation of Beckman Coulter Inc.’s corrective actions in response to our Warning Letter (CMS # 678042, March 2024). 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.
Sincerely,
/S/
Matthew G. Hillebrenner
Deputy Director
Office of Product Evaluation and Quality
Center for Devices and Radiological Health