# FDA Inspection 1102736 - Nexus CMF, LLC - September 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/89cd6387-d2f5-4742-bb08-06abeb2cc6f7
Source feed: FDA_Inspections

> FDA Inspection 1102736 for Nexus CMF, LLC on September 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102736
- Company Name: Nexus CMF, LLC
- Inspection Date: 2019-09-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102736 - 2019-09-25](https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/2ad5dc31-97bf-4593-90d6-c1388628430a)
- [FDA Inspection 950339 - 2015-10-01](https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/17379cbe-b0ce-4771-b77c-77b75cb8dc49)
- [FDA Inspection 950339 - 2015-10-01](https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/f9bd283f-cf7c-4fc0-a48b-fc4b654d9c75)
- [FDA Inspection 830380 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/89cd70b4-5f37-4a71-a826-58faf40cb598)
- [FDA Inspection 830380 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/nexus-cmf-llc/0817f158-3909-49fb-84a1-c9d6ab45716e)

Company: https://www.keypedia.com/companies/nexus-cmf-llc/55768276-0646-4b4a-aab0-8faf00a15af6

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