FDA Inspection 1024360 - Amplion Clinical Communications, Inc. - September 07, 2017

Record Details

This FDA Inspection record concerns Amplion Clinical Communications, Inc., with an inspection on September 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Amplion Clinical Communications, Inc.
Inspection Date: September 7, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9b2a4de4-ecd0-43f5-a382-a5dfc11920dc

Violation Codes10

21 CFR 806.20(a)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.12021 CFR 820.198(a)21 CFR 820.30(c)21 CFR 820.30(d)21 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.30(h)

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FDA Inspection

Amplion Clinical Communications, Inc.September 7, 2017

FDA Inspection 1024360 - Amplion Clinical Communications, Inc. - September 07, 2017

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Record Details

This FDA Inspection record concerns Amplion Clinical Communications, Inc., with an inspection on September 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Amplion Clinical Communications, Inc.
Inspection Date: September 7, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 9b2a4de4-ecd0-43f5-a382-a5dfc11920dc

Violation Codes10

21 CFR 806.20(a)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.12021 CFR 820.198(a)21 CFR 820.30(c)21 CFR 820.30(d)21 CFR 820.30(e)21 CFR 820.30(g)21 CFR 820.30(h)

Full citation text and observation details available on the Dashboard.