FDA Inspection 887569 - Medicomp, Inc. dba ReactDX - July 16, 2014

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Record Details

This FDA Inspection record concerns Medicomp, Inc. dba ReactDX, with an inspection on July 16, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medicomp, Inc. dba ReactDX
Inspection Date: July 16, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 29409266-31d0-4d6d-930a-057bfcf3e751

Violation Codes4

21 CFR 803.17(a)(3)21 CFR 820.198(a)21 CFR 820.30(g)21 CFR 820.50

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