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FDA Variance Application from Aquatic Multimedia LLC

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Summary

The FDA has posted a variance application from Aquatic Multimedia LLC. This document, submitted by CDRH, is available for review on the Regs.gov platform. No further details on the nature of the variance or its implications are provided in the available information.

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

What changed

The Food and Drug Administration (FDA) has made publicly available a variance application submitted by Aquatic Multimedia LLC. The application was posted on March 24, 2026, and is associated with docket number FDA-2025-V-5800-0001. The document was authored by the Center for Devices and Radiological Health (CDRH).

As this is a variance application, it is likely related to specific regulatory requirements for medical devices or pharmaceuticals. Compliance officers should note the docket number for tracking purposes and review the full application if it pertains to their organization's products or operations. No compliance deadlines or specific actions are indicated at this stage, as the document appears to be a submission for review rather than a final rule or guidance.

Archived snapshot

Mar 25, 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

There are no documents available to view or download

Attachments 1

Variance Application from Aquatic Multimedia LLC

More Information
- Author(s) CDRH
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Last updated

Classification

Agency
FDA
Published
March 24th, 2026
Instrument
Guidance
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2025-V-5800-0001
Docket
FDA-2025-V-5800-0001

Who this affects

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

Taxonomy

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

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