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FDA Variance Application from Illuminate Production Services

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Summary

The FDA has posted a variance application from Illuminate Production Services. The document is available for review on Regs.gov, with the application submitted by 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 posted a variance application submitted by Illuminate Production Services. The application, authored by CDRH, is available for public review via the Regs.gov portal. No specific details regarding the nature of the variance or the product/process it pertains to are provided in the initial document summary.

Given the limited information and the routine nature of variance applications, immediate action is likely not required for most regulated entities. Compliance officers should note the docket number for tracking purposes and review the full application if it pertains to their specific product or operational area. No compliance deadlines or penalties are associated with this notice.

Archived snapshot

Mar 21, 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 Illuminate Production Services

More Information
- Author(s) CDRH
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Last updated

Classification

Agency
FDA
Published
March 20th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2025-V-7067-0001
Docket
FDA-2025-V-7067-0001

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Product Approval
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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