FDA Inspection 735640 - OXFORD IMMUNOTEC INC DBA IMUGEN - July 21, 2011

FDA Inspection 735640 for OXFORD IMMUNOTEC INC DBA IMUGEN on July 21, 2011. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 735640 for OXFORD IMMUNOTEC INC DBA IMUGEN on July 21, 2011. Classification: No Action Indicated (NAI).

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Record Information

Company

OXFORD IMMUNOTEC INC DBA IMUGEN

Inspection Date

July 21, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fca33f35-48b1-426b-814e-8bbf5634ac16

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