FDA — OMEGA Letter: Interim Response, July 22, 2005


Date: July 22, 2005

Jay Davis, President 
Omega Laboratories, Inc. 400

RE: Request for Correction (Removal) of Information Found On the OrVD Section of the FDA Web Site

Dear Mr. Davis:

This letter is an interim response to your request for correction of information pursuant to the Federal Data Quality Act [Section 515(a) of the Treasury and General Government Appropriations Act for Fiscal Year 200 I, Pub. L. No.1 06-554, 114 Stat. 2763A-153 (2000)],  HHS Information Quality Guidelines and the FDA's Guidelines for Ensuring the Quality of Information Disseminated to the Public. Your request was received electronically on May 23, 2005.

The goal of the Food and Drug Administration (FDA) is to respond to such requests within 60 days. We are preparing a response to your request but will need more time to coordinate Agency review. We anticipate that a response will be forwarded to you by September 20,2005.


Laurie Lenkel 
Office of the Ombudsman Food and Drug Administration