American Bottling Co. - Keurig Dr Pepper FDA Record

Summary

FDA record by year

American Bottling Co. - Keurig Dr Pepper's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

American Bottling Co. - Keurig Dr Pepper FDA Warning Letters

1 warning letter on Jul 12, 2012.

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

7 inspections from Sep 17, 2009 to Apr 28, 2026.

NAI

No objectionable conditions or practices were found during the inspection.

VAI

Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.

OAI

Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under American Bottling Co. - Keurig Dr Pepper: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jul 12, 2012.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

American Bottling Co. - Keurig Dr Pepper and the FDA: common questions

Has American Bottling Co. - Keurig Dr Pepper received an FDA warning letter?

Yes. FDA has issued 1 warning letter to American Bottling Co. - Keurig Dr Pepper. The most recent is dated Jul 12, 2012.

Has American Bottling Co. - Keurig Dr Pepper received an FDA Form 483?

FDA has not published a Form 483 for "American Bottling Co. - Keurig Dr Pepper" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect American Bottling Co. - Keurig Dr Pepper?

The most recent FDA inspection on file ended Apr 28, 2026 at Irving, TX and was classified NAI. FDA has 7 inspections of American Bottling Co. - Keurig Dr Pepper on file, 1 of them classified OAI (official action indicated).