FDA Inspection 821656 - Exel, Inc. - February 21, 2013

FDA Inspection 821656 for Exel, Inc. on February 21, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 821656 for Exel, Inc. on February 21, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.160(a)

21 CFR 820.80(b)

21 CFR 820.90(a)

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Record Information

Company

Exel, Inc.

Inspection Date

February 21, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb2eb334-68f9-4f96-b9e3-b6672c3aaa7d

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