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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>8</VOL>
    <DATE>2000-04-01</DATE>
    <ORIGINALDATE>2000-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Servicing.</TITLE>
    <GRANULENUM>820.200</GRANULENUM>
    <HEADING>Section 820.200</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="4">Food and Drugs</PARENT>
      <PARENT HEADING="" SEQ="3"/>
      <PARENT HEADING="SUBCHAPTER H" SEQ="2">MEDICAL DEVICES</PARENT>
      <PARENT HEADING="PART 820" SEQ="1">QUALITY SYSTEM REGULATION</PARENT>
      <PARENT HEADING="Subpart N" SEQ="0">Servicing</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 820.200</SECTNO>
    <SUBJECT>Servicing.</SUBJECT>
    <P>(a) Where servicing is a specified requirement, each manufacturer shall establish and maintain instructions and procedures for performing and verifying that the servicing meets the specified requirements.</P>
    <P>(b) Each manufacturer shall analyze service reports with appropriate statistical methodology in accordance with § 820.100.</P>
    <P>(c) Each manufacturer who receives a service report that represents an event which must be reported to FDA under part 803 or 804 of this chapter shall automatically consider the report a complaint and shall process it in accordance with the requirements of § 820.198.</P>
    <P>(d) Service reports shall be documented and shall include:</P>
    <P>(1) The name of the device serviced;</P>
    <P>(2) Any device identification(s) and control number(s) used;</P>
    <P>(3) The date of service;</P>
    <P>(4) The individual(s) servicing the device;</P>
    <P>(5) The service performed; and</P>
    <P>(6) The test and inspection data.</P>
  </SECTION>
</CFRGRANULE>
