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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>1</VOL>
    <DATE>2003-04-01</DATE>
    <ORIGINALDATE>2003-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Product jurisdiction officer.</TITLE>
    <GRANULENUM>3.6</GRANULENUM>
    <HEADING>Section 3.6</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="4">Food and Drugs</PARENT>
      <PARENT HEADING="CHAPTER I" SEQ="3">FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES</PARENT>
      <PARENT HEADING="SUBCHAPTER A" SEQ="2">GENERAL</PARENT>
      <PARENT HEADING="PART 3" SEQ="1">PRODUCT JURISDICTION</PARENT>
      <PARENT HEADING="Subpart A" SEQ="0">Assignment of Agency Component for Review of Premarket Applications</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 3.6</SECTNO>
    <SUBJECT>Product jurisdiction officer.</SUBJECT>
    <P>FDA Ombudsman (HF-7), Food and Drug Administration, rm. 14-84, 5600 Fishers Lane, Rockville, MD 20857, 301-443-1306, is the designated product jurisdiction officer.</P>
  </SECTION>
</CFRGRANULE>
