# FDA Inspection 1029758 - Medicomp, Inc. dba ReactDX - October 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/medicomp-inc-dba-reactdx/62fcb57e-ffff-47c5-b84f-e681519879b0
Source feed: FDA_Inspections

> FDA Inspection 1029758 for Medicomp, Inc. dba ReactDX on October 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029758
- Company Name: Medicomp, Inc. dba ReactDX
- Inspection Date: 2017-10-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/medicomp-inc-dba-reactdx/bf31b52a-74fa-446d-9c3f-4f2470e249a2

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