# Relevium Labs Inc - Inspection Records

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

> Inspection records and compliance data for Relevium Labs Inc in Oxford, Ohio. Access full analysis and detailed observations.

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## Details

- Name: Relevium Labs Inc
- FEI Number: 3012697062
- City: Oxford
- State: Ohio
- Country Name: United States
- Address Line 1: 4663 Katie Ln Ste O
- Zip Code: 45056

## Related Documents

- [FDA Inspection 1261641 - Relevium Labs Inc - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/0d561fbb-aeed-401b-a35b-31c145dbb49c) — source: FDA, date: February 12, 2025
- [FDA Inspection 1261641 - Relevium Labs Inc - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/74e06523-b0a8-4657-818a-95414af4d923) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2025
- [FDA Inspection 1261641 - Relevium Labs Inc - 2025-02-12](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/36debde6-f6d1-4e18-b131-9312d55facbb) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2025
- [FDA Inspection 1179394 - Relevium Labs Inc - 2022-08-31](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/56e0faec-cc40-4b34-b948-6eb184f58406) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2022
- [FDA Inspection 1179394 - Relevium Labs Inc - 2022-08-31](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/eef8013a-d0fa-4300-84d4-43d1da43b27e) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2022
- [FDA Inspection 1031109 - Relevium Labs Inc - 2017-10-20](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/33b4e652-ef93-4a86-bd3f-1c90b8f9de93) — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2017
- [FDA Inspection 1031109 - Relevium Labs Inc - 2017-10-20](https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/c713c4de-a77a-4cde-ad7c-6fe55afd5ce3) — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2017

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