# Keurig Dr. Pepper (NASDAQ: KDP), Holland, MI – FDA Inspections

Source: https://www.keypedia.com/companies/keurig-dr-pepper/a7e86f26-6e75-467c-a7c6-70d10eff9e1f

> Inspection records and compliance data for Keurig Dr. Pepper in Holland, Michigan. 5 FDA inspections on record, 3 Form 483s, last inspected September 29, 2023. Publicly traded as NASDAQ: KDP.

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## Details

- Name: Keurig Dr. Pepper
- FEI Number: 3004274340
- Address Line 1: 777 Brooks Ave
- City: Holland
- State: Michigan
- Zip Code: 49423
- Country Name: United States
- Address: 777 Brooks Ave, Holland, Michigan 49423, United States
- Country: United States

## Stock

- Stock ticker: KDP
- Exchange: NASDAQ
- Share price: $36.92
- Market cap: $50.2B
- Price as of: November 6, 2026

## Related Documents

- [FDA Inspection 1219430 - Keurig Dr. Pepper - 2023-09-29](https://www.keypedia.com/records/fda_inspections/keurig-dr-pepper/ac5c31e5-a536-4355-9faa-ed541c970846) — source: FDA, date: September 29, 2023
- [FDA Inspection 1210434 - Keurig Dr. Pepper - 2023-07-19](https://www.keypedia.com/records/fda_inspections/keurig-dr-pepper/86bc7ca4-6bb7-4ae2-90aa-cc34618d555d) — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2023
- [FDA Inspection 995509 - Keurig Dr. Pepper - 2016-12-08](https://www.keypedia.com/records/fda_inspections/keurig-dr-pepper/fb4f8b7d-786e-4a0d-929f-b8958bf4c3e5) — source: FDA, date: December 8, 2016
- [FDA Inspection 862165 - Keurig Dr. Pepper - 2014-01-15](https://www.keypedia.com/records/fda_inspections/keurig-dr-pepper/bde6fefa-a258-41b7-b9ca-2f97c1714abe) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2014
- FDA Inspection 862165 - Keurig Dr. Pepper - 2014-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2014
- FDA Inspection 862165 - Keurig Dr. Pepper - 2014-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2014
- FDA Inspection 768564 - Keurig Dr. Pepper - 2012-02-23 — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2012

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