Guidance for industry and for FDA staff enforcement priorities for single-use devices reprocessed by third parties and hospitals.
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(2000). Guidance for industry and for FDA staff: enforcement priorities for single-use devices reprocessed by third parties and hospitals . U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance.
Chicago / Turabian - Author Date Citation, 17th Edition (style guide)2000. Guidance for Industry and for FDA Staff: Enforcement Priorities for Single-use Devices Reprocessed By Third Parties and Hospitals. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance.
Chicago / Turabian - Humanities (Notes and Bibliography) Citation, 17th Edition (style guide)Guidance for Industry and for FDA Staff: Enforcement Priorities for Single-use Devices Reprocessed By Third Parties and Hospitals U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance, 2000.
MLA Citation, 9th Edition (style guide)Guidance for Industry and for FDA Staff: Enforcement Priorities for Single-use Devices Reprocessed By Third Parties and Hospitals U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance, 2000.
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Grouping Information
Grouped Work ID | 2e0d31a5-b1f1-20ed-c762-cc6914442528-eng |
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Full title | guidance for industry and for fda staff enforcement priorities for single use devices reprocessed by third parties and hospitals |
Author | center for devices and radiological health |
Grouping Category | book |
Last Update | 2023-05-03 16:19:45PM |
Last Indexed | 2024-06-15 23:11:34PM |
Book Cover Information
Image Source | default |
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First Loaded | Feb 19, 2024 |
Last Used | Feb 19, 2024 |
Marc Record
First Detected | Dec 04, 2000 12:00:00 AM |
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Last File Modification Time | May 03, 2023 04:22:51 PM |
MARC Record
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245 | 0 | 0 | |a Guidance for industry and for FDA staff|h [electronic resource] :|b enforcement priorities for single-use devices reprocessed by third parties and hospitals. |
246 | 3 | 0 | |a Enforcement priorities for single-use devices reprocessed by third parties and hospitals |
260 | |a [Rockville, Md.] :|b U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance,|c [2000] | ||
500 | |a "Document issued on: August 14, 2000." | ||
500 | |a Distributed to depository libraries in microfiche on shipping list no.: 2002-0144-M. | ||
500 | |a Title from title screen (viewed on March 7, 2001). | ||
500 | |a GPO Cataloging Record Distribution Program (CRDP). | ||
538 | |a Mode of access: Internet from the U.S. Dept. of Health and Human Services | ||
650 | 0 | |a Disposable medical devices|z United States|v Handbooks, manuals, etc. | |
710 | 2 | |a Center for Devices and Radiological Health (U.S.).|b Office of Compliance. | |
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