Changeflow GovPing Healthcare FDA Variance Application from Kenyon Production...
Routine Notice Removed Final

FDA Variance Application from Kenyon Productions, LLC Closed

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Summary

The Food and Drug Administration (FDA) has closed a variance application submitted by Kenyon Productions, LLC. The specific details of the variance and the reasons for its closure are not provided in the available document.

What changed

The FDA has officially closed a variance application submitted by Kenyon Productions, LLC. The document indicates that the application, associated with docket number FDA-2026-V-1632, is no longer active. No specific details regarding the nature of the variance, the product involved, or the reasons for the closure are available in the provided information.

Given the closure of the application, there are no immediate compliance actions required for other regulated entities. This notice serves as an administrative update. Companies considering or currently undergoing similar variance application processes should note that this specific application has been resolved, but the underlying regulatory pathways remain in place.

Source document (simplified)

Content

There are no documents available to view or download

Attachments 1

Variance Application from Kenyon Productions, LLC

More Information
- Author(s) CDRH
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Classification

Agency
FDA
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2026-V-1632-0001

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
Topics
Medical Devices

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