FDA Inspection 1071013 - Norfolk Medical Products, Inc. - November 02, 2018

FDA Inspection 1071013 for Norfolk Medical Products, Inc. on November 02, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1071013 for Norfolk Medical Products, Inc. on November 02, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.30(g)

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Record Information

Company

Norfolk Medical Products, Inc.

Inspection Date

November 2, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f70938c8-f091-4016-ba24-5eec3f51d1e8

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