# FDA 483 - CGR Products MN, LLC. - March 12, 2026

Source: https://www.keypedia.com/records/483/cgr-products-mn-llc/6cca1920-fc3a-4367-a7db-7446144d8137

> FDA 483 for CGR Products MN, LLC. on March 12, 2026. Product: other. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: CGR Products MN, LLC.
- Inspection Date: 2026-03-12
- Product Type: other
- Office Name: Minneapolis District Office
- Summary: An FDA inspection of CGR Products MN, LLC, a manufacturer of sterile seal devices in Inver Grove Heights, MN, revealed significant deficiencies in their quality system. The firm failed to adequately document production controls, including process parameters and adjustments for lamination and slitting processes. Additionally, records for nonconforming products and the effectiveness of corrective actions were not properly maintained.

## Related Officers

- [Albert L. Nguyen](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)

Company: https://www.keypedia.com/companies/cgr-products-mn-llc/c60be532-69a3-4bd4-85d0-1eb16ce485b7

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d