FDA Inspection 1217172 - Medicomp, Inc. dba ReactDX - August 30, 2023

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Record Details

This FDA Inspection record concerns Medicomp, Inc. dba ReactDX, with an inspection on August 30, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medicomp, Inc. dba ReactDX
Inspection Date: August 30, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4c1e7d99-7429-4d8d-bed3-29acd3edc83d