FDA Inspection 586544 - Tornier, Inc - May 14, 2009

FDA Inspection 586544 for Tornier, Inc on May 14, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 586544 for Tornier, Inc on May 14, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(1)

21 CFR 820.100(b)

21 CFR 820.40(b)

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Record Information

Company

Tornier, Inc

Inspection Date

May 14, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb28416b-4e7f-4472-b66f-fb3ab1622e93

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