FDA Inspection 676597 - Verticor, Ltd - August 05, 2010

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Record Details

This FDA Inspection record concerns Verticor, Ltd, with an inspection on August 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Verticor, Ltd
Inspection Date: August 5, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 35ba3992-9769-4864-8ce1-8b423a2f2635

Violation Codes4

21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)

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