FDA Inspection 753559 - Anchorplus - November 08, 2011

FDA Inspection 753559 for Anchorplus on November 08, 2011. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 753559 for Anchorplus on November 08, 2011. Classification: No Action Indicated (NAI).

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Record Information

Company

Anchorplus

Inspection Date

November 8, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fda1885a-b392-4f7b-b164-0e4eed8d29f5

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