FDA Inspection 630672 - Zimmer Spine, Inc. - November 06, 2009

FDA Inspection 630672 for Zimmer Spine, Inc. on November 06, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 630672 for Zimmer Spine, Inc. on November 06, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 806.10(b)

21 CFR 820.198(a)(1)

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Record Information

Company

Zimmer Spine, Inc.

Inspection Date

November 6, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fca1ff08-2b86-4d9f-8984-4c23957dce29

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