FDA Inspection 596268 - Axiom Worldwide,Inc. - July 10, 2009

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Record Details

This FDA Inspection record concerns Axiom Worldwide,Inc., with an inspection on July 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Axiom Worldwide,Inc.
Inspection Date: July 10, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 495a6bd4-471b-45bc-a89d-d926effbeee2

Violation Codes5

21 CFR 820.100(a)(1)21 CFR 820.100(a)(4)21 CFR 820.198(c)21 CFR 820.50(a)(2)21 CFR 820.70(a)

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