FDA Inspection 935190 - Dukal Llc - July 13, 2015

FDA Inspection 935190 for Dukal Llc on July 13, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 935190 for Dukal Llc on July 13, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Dukal Llc

Inspection Date

July 13, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7ea1513-7a06-4fb2-9fbf-6acf9cf34e2e

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