# Kwik Trip, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/kwik-trip-inc/70590949-c1aa-4e94-90a4-79da25847aa9

> Inspection records and compliance data for Kwik Trip, Inc. in La Crosse, Wisconsin. 8 FDA inspections on record, last inspected October 23, 2024.

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## Details

- Name: Kwik Trip, Inc.
- FEI Number: 2127538
- Address Line 1: 2200 Palace Street
- City: La Crosse
- State: Wisconsin
- Zip Code: 54602
- Country Name: United States
- Address: 2200 Palace Street, La Crosse, Wisconsin 54602, United States
- Country: United States

## Related Documents

- FDA Inspection 1254541 - Kwik Trip, Inc. - 2024-10-23 — source: FDA, date: October 23, 2024
- FDA Inspection 1254541 - Kwik Trip, Inc. - 2024-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2024
- FDA Inspection 1254541 - Kwik Trip, Inc. - 2024-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2024
- FDA Inspection 1226671 - Kwik Trip, Inc. - 2023-12-07 — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2023
- FDA Inspection 1174797 - Kwik Trip, Inc. - 2022-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2022
- FDA Inspection 1106626 - Kwik Trip, Inc. - 2019-08-26 — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2019
- [FDA Inspection 995266 - Kwik Trip, Inc. - 2016-11-23](https://www.keypedia.com/records/fda_inspections/kwik-trip-inc/633e4630-dbd8-4ded-896e-e9cc95cc2625) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 23, 2016
- FDA Inspection 868644 - Kwik Trip, Inc. - 2014-02-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 5, 2014
- [FDA Inspection 733087 - Kwik Trip, Inc. - 2011-07-01](https://www.keypedia.com/records/fda_inspections/kwik-trip-inc/2d88a24a-aaed-470d-a6bc-09547fce62a8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2011
- FDA Inspection 648888 - Kwik Trip, Inc. - 2010-02-19 — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2010

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