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GAO-08-769R 1 (2008-05-16)

handle is hein.gao/gaobadwtm0001 and id is 1 raw text is: 


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T V   WAccountability * Integrity * Reliability
United States Government Accountability Office
Washington, DC 20548

          B-316426


          May 16, 2008

          The Honorable Edward M. Kennedy
          Chairman
          The Honorable Michael B. Enzi
          Ranking Minority Member
          Committee on Health, Education, Labor, and Pensions
          United States Senate

          The Honorable John D. Dingell
          Chairman
          The Honorable Joe Barton
          Ranking Minority Member
          Committee on Energy and Commerce
          House of Representatives

          Subject: Department of Health and Human Services, Food and DrugAdministration:
                  Substances Prohibited From Use in Animal Food or Feed

          Pursuant to section 801(a)(2)(A) of title 5, United States Code, this is our report on a
          major rule promulgated by the Department of Health and Human Services, Food and
          Drug Administration (FDA), entitled Substances Prohibited From Use in Animal
          Food or Feed (RIN: 0910-AF46). We received the rule on May 2, 2008. It was
          published in the Federal Register as a final rule on April 25, 2008. 73 Fed. Reg.
          22,720.

          The final rule prohibits the use of certain cattle origin materials in the food or feed of
          all animals to further reduce the risk of the spread of bovine spongiform
          encephalopathy (BSE) within the United States. FDA states that the intent of the
          final rule is to strengthen the safeguards designed to prevent the spread of BSE in
          U.S. cattle, as well as to reduce further any risk posed to humans from the agent that
          causes BSE. The final rule is effective on April 27, 2009.

          Enclosed is our assessment of the FDA's compliance with the procedural steps
          required by section 801(a)(1)(B)(i) through (iv) of title 5 with respect to the rule.
          Our review indicates that FDA complied with the applicable requirements.


GAO-08-769R

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