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Open for comment Health and Human Services Department, Food and Drug Administration Docket Docket No. FDA-2026-N-8482

FDA seeks public comment on proposed information collection for allegations of regulatory misconduct submitted to CDRH

💬 Comments close in 21 days (Oct 26)

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Timeline

  1. Proposed / opened

    FDA seeks public comment on proposed information collection for allegations of regulatory misconduct submitted to CDRH

  2. Related document

    Agency Information Collection Activities; Proposed Collection; Comment Request; Allegations of Regulatory Misconduct Voluntarily Submitted to the Center for Devices and Radiological Health

Briefs in this proceeding

FYI FDA 💬 Comments close in 21 days (Oct 26)

FDA seeks public comment on proposed information collection for allegations of regulatory misconduct submitted to CDRH

This notice allows stakeholders to comment on FDA's plan to collect and manage voluntary reports of regulatory misconduct involving medical devices and radiological health products. The Food and Drug Administration (FDA) has published a notice in the Federal Register announcing a 60-day public...

Sources

Health and Human Services Department, Food and Drug Administration · Agency Information Collection Activities; Proposed Collection; Comment Request; Allegations of Regulatory Misconduct Voluntarily Submitted to the Center for Devices and Radiological Health · Aug 26