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483
•OneBlood, Inc.•April 18, 2019

FDA 483 - OneBlood, Inc. - April 18, 2019

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Record Details

An FDA inspection of OneBlood, Inc. in Pensacola, FL, a community blood center, identified a significant issue during a mobile blood drive. The firm failed to provide adequate private space for individuals to complete computer-assisted self-interviews to determine their eligibility as blood donors. This condition could compromise the accuracy and privacy of sensitive donor screening information.

Company
OneBlood, Inc.
Inspection Date
April 18, 2019
Product Type
Biologics
Office
Office of Medical Device and Radiological Health Division II
Person
  • Jason D Abel
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ID · 58a7444a-d23b-4763-ba9e-7556347c7bf2

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