FDA Inspection 866686 - BD - January 31, 2014

FDA Inspection 866686 for BD on January 31, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 866686 for BD on January 31, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Inspection Date

January 31, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd72d41f-41ce-4ba4-8e95-8a47cf750f30

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