# Relevium Labs Inc – FDA Inspection, Oct 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/relevium-labs-inc/c713c4de-a77a-4cde-ad7c-6fe55afd5ce3
Source feed: FDA_Inspections

> FDA inspection 1031109 of Relevium Labs Inc, October 20, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1031109
- Company Name: Relevium Labs Inc
- Inspection Date: 2017-10-20
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1261641 - 2025-02-12
- FDA Inspection 1179394 - 2022-08-31

## Related Officers

- Teresa K. Kastner

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