# Grand River Aseptic Manufacturing Inc. – FDA Inspection, Nov 4, 2025

Source: https://www.keypedia.com/records/fda_inspections/grand-river-aseptic-manufacturing-inc/508b1f53-f3ac-42d4-b505-f60b05439e55
Source feed: FDA_Inspections

> FDA inspection 1293366 of Grand River Aseptic Manufacturing Inc., November 04, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 211. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1293366
- Company Name: Grand River Aseptic Manufacturing Inc.
- Inspection Date: 2025-11-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Detroit District Office
- Citation Count: 2

## Related Documents

- FDA Inspection 1236900 - 2024-02-21
- [FDA Inspection 1219116 - 2023-09-29](https://www.keypedia.com/records/fda_inspections/grand-river-aseptic-manufacturing-inc/0e3ef469-b76f-4460-914a-3b98e79d3c70)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jacob-g-lutz/ca2710c6-064f-4728-9129-aad73e74f12d)

Company: https://www.keypedia.com/companies/grand-river-aseptic-manufacturing-inc/f538a5fa-320e-4240-954d-762b7d02795a

Office: https://www.keypedia.com/offices/detroit-district-office/b09a1815-a000-40c0-bb44-5432ce87ed03