Franklin

The Food and Drug Administration's policies and procedures should better address postmarket cybersecurity risk to medical devices.

Publication:
[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2018.
Format/Description:
Government document
Book
1 online resource (29 pages)
Subjects:
Medical instruments and apparatus -- Safety regulations -- United States.
United States. Department of Health and Human Services. Office of Inspector General -- Auditing.
Computer security -- United States.
Notes:
"October 2018."
"A-18-16-30530."
CRDP Program record.
Description based on online resource; title from PDF title page (U.S. Department of Health and Human Services website, viewed Nov. 2, 2018).
Contributor:
United States. Department of Health and Human Services. Office of Inspector General, issuing body.
OCLC:
1060614971
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