# FDA Inspection 1031109 - Relevium Labs Inc - October 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/33b4e652-ef93-4a86-bd3f-1c90b8f9de93
Source feed: FDA_Inspections

> FDA Inspection 1031109 for Relevium Labs Inc on October 20, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1031109
- Company Name: Relevium Labs Inc
- Inspection Date: 2017-10-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1261641 - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/0d561fbb-aeed-401b-a35b-31c145dbb49c)
- [FDA Inspection 1261641 - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/36debde6-f6d1-4e18-b131-9312d55facbb)
- [FDA Inspection 1261641 - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/74e06523-b0a8-4657-818a-95414af4d923)
- [FDA Inspection 1179394 - 2022-08-31](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/eef8013a-d0fa-4300-84d4-43d1da43b27e)
- [FDA Inspection 1179394 - 2022-08-31](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/56e0faec-cc40-4b34-b948-6eb184f58406)

Company: https://www.keypedia.com/companies/relevium-labs-inc/50181260-7765-46a1-80a8-3fb832152195

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