# FDA Inspection 1308058 - CGR Products MN, LLC. - March 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 for CGR Products MN, LLC. on March 12, 2026. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1308058 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/77944c88-d14d-42c2-886d-fa608bacb5e6)
- [FDA Inspection 1165415 - 2022-03-02](https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/5e50174c-0e2d-4559-8f7d-51a13cd1bbf8)
- [FDA Inspection 1165415 - 2022-03-02](https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/8e6f3341-8ce2-4eea-92f4-8a1db870b690)
- [FDA Inspection 1032347 - 2017-11-15](https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/3d4b2220-4ede-45a8-85bf-be4c9e540b56)

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