FDA Inspection 583580 - Alken Inc. Dba Polhemus - May 08, 2009

FDA Inspection 583580 for Alken Inc. Dba Polhemus on May 08, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 583580 for Alken Inc. Dba Polhemus on May 08, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Alken Inc. Dba Polhemus

Inspection Date

May 8, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff963238-5166-4727-8afc-cfb035fc4e0b

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