# Dymedix Diagnostics, Inc. – FDA Inspection, Oct 14, 2021

Source: https://www.keypedia.com/records/fda_inspections/dymedix-diagnostics-inc/d30f14f6-6657-4731-81c9-4385c8730aad
Source feed: FDA_Inspections

> FDA inspection 1156518 of Dymedix Diagnostics, Inc., October 14, 2021. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1156518
- Company Name: Dymedix Diagnostics, Inc.
- Inspection Date: 2021-10-14
- 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 1304040 - 2026-02-11
- FDA Inspection 980290 - 2016-07-07
- FDA Inspection 793237 - 2012-08-02

Company: https://www.keypedia.com/companies/dymedix-diagnostics-inc/b33b04ec-c1a3-4733-928b-33bb647402bb

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