- Teleflex Medical
- Issuing Office:
Department of Health and Human Services
|Food and Drug Administration|
550 West Jackson Blvd., 15th Floor
Chicago, Illinois 60661
September 14, 2015
VIA UPS NEXT DAY
Mr. Benson F. Smith
550 E. Swedes Ford Road, Suite 400
Wayne, PA 19087
Dear Mr. Smith:
The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter, CHI-05-14 dated March 11, 2014. 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.
William R. Weissinger