FDA Inspection 621663 - Arthrex, Inc. - October 09, 2009

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Record Details

This FDA Inspection record concerns Arthrex, Inc., with an inspection on October 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Arthrex, Inc.
Inspection Date: October 9, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 69b01e82-4598-4d2f-9f4b-284f2dbb8b4d

Violation Codes8

21 CFR 820.100(a)21 CFR 820.20(b)21 CFR 820.25(b)21 CFR 820.30(c)21 CFR 820.30(d)21 CFR 820.30(e)21 CFR 820.30(i)21 CFR 820.40(a)

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