Changeflow GovPing Healthcare FDA Acknowledgment Letter to Laina Callow
Routine Notice Added Final

FDA Acknowledgment Letter to Laina Callow

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Summary

The Food and Drug Administration (FDA) has issued an acknowledgment letter to Laina Callow regarding a submission. The document is a redacted version of an acknowledgment letter from the FDA's Division of Management and Budget (DMB) to Laina Callow, authored by CDRH.

Published by FDA on regulations.gov . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

The FDA has posted a redacted acknowledgment letter sent to Laina Callow. This document, authored by the Center for Devices and Radiological Health (CDRH) and the Division of Management and Budget (DMB), serves as official confirmation of receipt for a submission.

While this is a routine administrative notice, regulated entities should be aware that such acknowledgments are part of the formal communication process with the FDA. Compliance officers should ensure that all necessary submissions are properly tracked and that acknowledgment letters are received and filed appropriately as part of their record-keeping obligations.

What to do next

  1. Ensure internal records reflect receipt of this acknowledgment if applicable to ongoing submissions.
  2. Review CDRH communication protocols for any updates or specific requirements.

Archived snapshot

Mar 27, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Content

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Attachments 2

Acknowledgment Letter from FDA DMB to Laina Callow

Restricted: Personally Identifiable Information

More Information
- Author(s) CDRH

Acknowledgment Letter from FDA DMB to Laina Callow - Redacted

More Information
- Author(s) CDRH
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Last updated

Classification

Agency
FDA
Published
March 26th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2026-V-1611-0002
Docket
FDA-2026-V-1611-0002

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Regulatory Submissions
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Compliance frameworks
FDA 21 CFR Part 11
Topics
Medical Devices

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