Research Catalog

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

Title
  1. The Food and Drug Administration's policies and procedures should better address postmarket cybersecurity risk to medical devices.
Published by
  1. [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2018.

Available online

Details

Additional authors
  1. United States. Department of Health and Human Services. Office of Inspector General, issuing body
Description
  1. 1 online resource (29 pages)
Subject
  1. United States. Department of Health and Human Services. Office of Inspector General > Auditing
  2. Medical instruments and apparatus > Safety regulations > United States
  3. Computer security > United States
Call number
  1. GPO Internet HE 1.2:M 46/29
Note
  1. "October 2018."
  2. "A-18-16-30530."
Source of description (note)
  1. Description based on online resource; title from PDF title page (U.S. Department of Health and Human Services website, viewed Nov. 2, 2018).
Title
  1. The Food and Drug Administration's policies and procedures should better address postmarket cybersecurity risk to medical devices.
Publisher
  1. [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2018.
Type of content
  1. text
Type of medium
  1. computer
Type of carrier
  1. online resource
Connect to:
  1. https://purl.fdlp.gov/GPO/gpo111086
Added author
  1. United States. Department of Health and Human Services. Office of Inspector General, issuing body.
Gpo item no.
  1. 0445 (online)
Sudoc no.
  1. HE 1.2:M 46/29
View in legacy catalog