# CCRM Minneapolis - Inspection Records

Source: https://www.keypedia.com/companies/ccrm-minneapolis/7d3251e9-a1ff-4658-8d3a-d30779b2eb50

> Inspection records and compliance data for CCRM Minneapolis in Edina, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: CCRM Minneapolis
- FEI Number: 3011394724
- City: Edina
- State: Minnesota
- Country Name: United States
- Address Line 1: 6565 France Ave S Ste 400
- Zip Code: 55435

## Related Documents

- [FDA Inspection 1277272 - CCRM Minneapolis - 2025-07-22](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/ee53fa74-8e62-4aeb-a838-1279b5a79b61) — source: FDA, date: July 22, 2025
- [FDA Inspection 1277272 - CCRM Minneapolis - 2025-07-22](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/fed71eab-c71e-4e39-ae3f-b8d748fbd65a) — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2025
- [FDA Inspection 1217004 - CCRM Minneapolis - 2023-07-27](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/ee2881cf-0923-4a34-a423-a27297bea88b) — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2023
- [FDA Inspection 1217004 - CCRM Minneapolis - 2023-07-27](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/9aebe406-5f73-42fb-af76-7e0026d3bc91) — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2023
- [FDA Inspection 1067222 - CCRM Minneapolis - 2018-08-31](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/23d8d0ad-9383-432d-bcc4-3c741a98f207) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2018
- [FDA Inspection 1067222 - CCRM Minneapolis - 2018-08-31](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/509d7c27-2c35-44c9-bb65-5e18e7ce584f) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2018
- [FDA Inspection 984898 - CCRM Minneapolis - 2016-09-08](https://www.keypedia.com/records/fda_inspections/ccrm-minneapolis/731128b3-6d7d-46f1-ae08-3f088b772057) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2016

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