FDA Inspection 930509 - Auric Enterprises, Inc. D.B.A. Diack - June 17, 2015

Record Details

This FDA Inspection record concerns Auric Enterprises, Inc. D.B.A. Diack, with an inspection on June 17, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Auric Enterprises, Inc. D.B.A. Diack
Inspection Date: June 17, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 62de23da-b293-4159-9238-897d781aa804

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.20(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(i)21 CFR 820.4021 CFR 820.5021 CFR 820.50(a)

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FDA Inspection

Auric Enterprises, Inc. D.B.A. DiackJune 17, 2015

FDA Inspection 930509 - Auric Enterprises, Inc. D.B.A. Diack - June 17, 2015

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Record Details

This FDA Inspection record concerns Auric Enterprises, Inc. D.B.A. Diack, with an inspection on June 17, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Auric Enterprises, Inc. D.B.A. Diack
Inspection Date: June 17, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 62de23da-b293-4159-9238-897d781aa804

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.20(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(i)21 CFR 820.4021 CFR 820.5021 CFR 820.50(a)

Full citation text and observation details available on the Dashboard.