FDA Inspection 811984 - ACell, Inc - December 20, 2012

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Record Details

This FDA Inspection record concerns ACell, Inc, with an inspection on December 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: ACell, Inc
Inspection Date: December 20, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a751a08c-3361-4b42-8dd6-a4761d6cb72e

Violation Codes3

21 CFR 803.50(a)(1)21 CFR 820.30(a)21 CFR 820.70(a)

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