FDA Inspection 805059 - Keurig Dr Pepper dba The American Bottling Company - October 25, 2012

FDA Inspection 805059 for Keurig Dr Pepper dba The American Bottling Company on October 25, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 805059 for Keurig Dr Pepper dba The American Bottling Company on October 25, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Keurig Dr Pepper dba The American Bottling Company

Inspection Date

October 25, 2012

Product Type

Food/Cosmetics

ID: fa9559c3-37d2-49e5-8736-cddeb4baba13

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