Inspections, Compliance, Enforcement, and Criminal Investigations
Anchor Products Company Close out Letter 10/27/11
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Public Health Service Food and Drug Administration |
| Chicago District 550 West Jackson Blvd., 15th Floor Chicago, Illinois 60661 Telephone: 312-353-5863 |
October 27, 2011
Robert H. Thrun, President
Anchor Products Company
52 Official Road
Addison, IL 60101-4589
Dear Mr. Thrun:
The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter CHI-01-11 dated November 8, 2010. 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 and 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/
Richard Harrison
Compliance Director





Department of Health and Human Services

