Changeflow GovPing Healthcare FDA Variance Application from Ingram Planetarium
Routine Notice Added Final

FDA Variance Application from Ingram Planetarium

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Summary

The Food and Drug Administration (FDA) has posted a variance application from Ingram Planetarium. The application is available for review on Regulations.gov, with the author listed as CDRH.

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 a variance application from Ingram Planetarium publicly available via Regulations.gov. The application, authored by CDRH, is associated with docket ID FDA-2026-V-1057-0001. This filing indicates a specific request for a deviation from standard FDA regulations for a particular entity.

Compliance officers should note this filing as an example of a variance application process. While this specific application is unlikely to impose direct obligations on other entities, it highlights the existence of mechanisms for seeking regulatory flexibility. No immediate actions are required for most regulated entities, but awareness of such applications can be useful for understanding regulatory interpretations and potential future policy shifts.

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 1

Variance Application from Ingram Planetarium

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-1057-0001
Docket
FDA-2026-V-1057-0001

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 Labeling
Geographic scope
United States US

Taxonomy

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

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