FDA Inspection 541038 - VertiFlex, Inc. - October 07, 2008

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Record Details

This FDA Inspection record concerns VertiFlex, Inc., with an inspection on October 7, 2008, issued by the Center for Devices and Radiological Health, covering devices.

Company: VertiFlex, Inc.
Inspection Date: October 7, 2008
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d2bbe648-2ed2-4cec-b912-2fb896e3bedf

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.100(a)(3)21 CFR 820.150(a)21 CFR 820.20(e)21 CFR 820.30(g)21 CFR 820.5021 CFR 820.70(a)21 CFR 820.72(a)21 CFR 820.72(b)(2)

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