# FDA Inspection 1032347 - CGR Products MN, LLC. - November 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/3d4b2220-4ede-45a8-85bf-be4c9e540b56
Source feed: FDA_Inspections

> FDA Inspection 1032347 for CGR Products MN, LLC. on November 15, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1032347
- Company Name: CGR Products MN, LLC.
- Inspection Date: 2017-11-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1308058 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/cgr-products-mn-llc/5d3fdca6-2391-48d8-8b81-73742d8966e2)
- [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)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7