# CGR Products MN, LLC. – FDA Inspection, Mar 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/5d3fdca6-2391-48d8-8b81-73742d8966e2
Source feed: FDA_Inspections

> FDA inspection 1308058 of CGR Products MN, LLC., March 12, 2026. Classification: Voluntary Action Indicated (VAI). 3 citations. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1308058
- Company Name: CGR Products MN, LLC.
- Inspection Date: 2026-03-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 3

## Related Documents

- FDA Inspection 1165415 - 2022-03-02
- FDA Inspection 1032347 - 2017-11-15

## Related Officers

- [Issuing Officer](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