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

Source: https://www.globalkeysolutions.net/records/fda_inspections/keurig-dr-pepper-dba-the-american-bottling-company/fa9559c3-37d2-49e5-8736-cddeb4baba13/
Source feed: FDA_Inspections

> 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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## Details

- Record Type: FDA Inspection
- Inspection ID: 805059
- Company Name: Keurig Dr Pepper dba The American Bottling Company
- Inspection Date: 2012-10-25
- Classification: No Action Indicated (NAI)
- Project Area: Foodborne Biological Hazards
- Product Type: Food/Cosmetics

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Company: https://www.globalkeysolutions.net/companies/keurig-dr-pepper-dba-the-american-bottling-company/b77a2061-67a7-496e-a542-ef9bdcccae63
