FDA Issues Draft Guidance on Discontinuance or Interruption of Manufacturing of Certain Devices Implementing CARES Act
Arnold Porter
JANUARY 24, 2022
You should consult with counsel to determine applicable legal requirements in a specific fact situation. This Draft Guidance, and the currently in place November 2020 Guidance, were prompted by shortages caused by the pandemic. Who Must Notify FDA Under 506J? © Arnold & Porter Kaye Scholer LLP 2022 All Rights Reserved.
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