CLOSEOUT LETTER
Alber GmbH
- Product:
- Medical Devices
- Recipient:
- Alber GmbH
United States
- Issuing Office:
United States
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10903 New Hampshire Avenue
Silver Spring, MD 20993 |
July 27, 2018
Hansjorg Reiner
Managing Director
Alber GmbH
Vor dem Weissen Stein 21
Albstadt, Germany 722461
Dear Mr. Reiner:
The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter [CMS Case #532755] dated September 15, 2017. 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/
William C. MacFarland
Director
Division of Manufacturing and Quality
Office of Compliance
Center for Devices and Radiological Health
CC:
US Agent
Elijah N. Wreh
Invacare Corporation
One Invacare Way
Elyria, OH 44035
Ewreh@invacare.com