The Food and Drug Administration's policies and procedures should better address postmarket cybersecurity risk to medical devices.
- [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2018.
- Government document
1 online resource (29 pages)
- 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.
- "October 2018."
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).
- United States. Department of Health and Human Services. Office of Inspector General, issuing body.
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