FDA WARNING_LETTER - Siemens Healthcare Diagnostics, Inc. - February 09, 2012

FDA WARNING_LETTER for Siemens Healthcare Diagnostics, Inc. on February 09, 2012. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Siemens Healthcare Diagnostics, Inc. on February 09, 2012. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.100(a)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.90(b)(2)

21 CFR 820.90(a)

21 U.S.C. 351(h)

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Record Information

Company

Siemens Healthcare Diagnostics, Inc.

Inspection Date

February 9, 2012

Product Type

Devices

Office

Philadelphia District Office

People

ID: fc024c83-d667-4698-853d-0e3e55b21c30

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