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

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

Bibliographic Details
Format: Government Document eBook
Language:English
Published: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2018.
Subjects:
United States. > Department of Health and Human Services. > Office of Inspector General > Auditing.
Medical instruments and apparatus > Safety regulations > United States.
Computer security > United States.
Online Access:https://purl.fdlp.gov/GPO/gpo111086

Internet

https://purl.fdlp.gov/GPO/gpo111086

Available Online

Holdings details from Available Online
Call Number: HE 1.2:M 46/29
 
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HE 1.2:M 46/29 Available