# FDA Inspection 1205951 - Keurig/Dr. Pepper - April 25, 2023

Source: https://www.keypedia.com/records/fda_inspections/keurigdr-pepper/97db5b79-1af2-41dd-9b2f-672cbcb6131c
Source feed: FDA_Inspections

> FDA Inspection 1205951 for Keurig/Dr. Pepper on April 25, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205951
- Company Name: Keurig/Dr. Pepper
- Inspection Date: 2023-04-25
- Classification: No Action Indicated (NAI)
- Project Area: Foodborne Biological Hazards
- Product Type: Food/Cosmetics
- Office Name: Center for Food Safety and Applied Nutrition

## Related Documents

- [FDA Inspection 909185 - 2014-12-10](https://www.keypedia.com/records/fda_inspections/keurigdr-pepper/984c3978-a070-4ba7-81bc-74fe132483d5)
- [FDA Inspection 848649 - 2013-09-04](https://www.keypedia.com/records/fda_inspections/keurigdr-pepper/3c679aeb-beae-4ced-8564-46978eda5f17)

Company: https://www.keypedia.com/companies/keurigdr-pepper/c932bf9c-52fb-403e-964f-931511561ed3

Office: https://www.keypedia.com/offices/center-for-food-safety-and-applied-nutrition/e04dc4e5-ee4f-4b0d-be8c-1139531ddab2