# FDA Inspection 980290 - Dymedix Diagnostics, Inc. - July 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/dymedix-diagnostics-inc/b4307a76-a208-46b3-bf5f-2b06f8ee4fb4
Source feed: FDA_Inspections

> FDA Inspection 980290 for Dymedix Diagnostics, Inc. on July 07, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980290
- Company Name: Dymedix Diagnostics, Inc.
- Inspection Date: 2016-07-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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