FDA Inspection 966845 - Follett, LLC - March 29, 2016

FDA Inspection 966845 for Follett, LLC on March 29, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 966845 for Follett, LLC on March 29, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

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Record Information

Company

Follett, LLC

Inspection Date

March 29, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7ced0c5-0e88-40ba-b6dd-a83bc908cd7c

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