rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Medical devices
    sub title: FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees
  title info:
    title: Medical devices
    sub title: Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process
  title info:
    title: Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process
  title info:
    title: Medical device premarket review
  name:
    name part: United States
    name part: Government Accountability Office.
    role:
      role term: creator
  type of resource: text
  genre: bibliography
  origin info:
    place:
      place term: dcu
    date issued: 2009
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: electronic
    form: remote
    extent: iv, 57 pages : digital, PDF file.
  note: Title from title screen (viewed Feb. 17, 2009).
  note: "January 2009."
  note: "GAO-09-190."
  note: Electronic resource.
  note: Mode of access: Internet from GAO web site. Address as of 2/17/09: http://www.gao.gov/new.items/d09190.pdf ; current access available via PURL.
  note: Includes bibliographical references.
  subject:
    geographic code: n-us---
  subject:
    name:
      name part: United States.
      name part: Food and Drug Administration
    topic: Management
  subject:
    name:
      name part: United States.
      name part: Food and Drug Administration.
  subject:
    topic: Medical instruments and apparatus
    topic: Standards
    geographic: United States
  subject:
    topic: Equipment and Supplies
    topic: standards
    geographic: United States
    genre: Statistics
  classification: GA 1.13:GAO-09-190
  related item:
    title info:
      title: Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process
    name:
      name part: United States. Government Accountability Office.
    physical description:
      extent: iv, 57 p.
    identifier: (OCoLC)300161424
  identifier: https://purl.fdlp.gov/GPO/LPS109040
  record info:
    record content source: GPO
    record creation date: 090226
    record change date: 20211202190845.0
    record identifier: in00002484832