FDA Inspection 926848 - RNK Products, Inc - May 20, 2015

FDA Inspection 926848 for RNK Products, Inc on May 20, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 926848 for RNK Products, Inc on May 20, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

RNK Products, Inc

Inspection Date

May 20, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f73a65ad-741e-41fc-9d87-2cdc9698ae34

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