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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>Equipment design.</TITLE>
    <GRANULENUM>58.61</GRANULENUM>
    <HEADING>Section 58.61</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 58" SEQ="1">GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES</PARENT>
      <PARENT HEADING="Subpart D" SEQ="0">Equipment</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 58.61</SECTNO>
    <SUBJECT>Equipment design.</SUBJECT>
    <P>Equipment used in the generation, measurement, or assessment of data and equipment used for facility environmental control shall be of appropriate design and adequate capacity to function according to the protocol and shall be suitably located for operation, inspection, cleaning, and maintenance.</P>
    <CITA>[52 FR 33780, Sept. 4, 1987]</CITA>
  </SECTION>
</CFRGRANULE>
