# Krispy Kreme Doughnut Corporation, Mishawaka, IN – FDA Inspections

Source: https://www.keypedia.com/companies/krispy-kreme-doughnut-corporation/c36591e4-483c-4563-a515-0266eb32ad0c

> Inspection records and compliance data for Krispy Kreme Doughnut Corporation in Mishawaka, Indiana. 7 FDA inspections on record, last inspected April 07, 2026.

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## Details

- Name: Krispy Kreme Doughnut Corporation
- FEI Number: 3004398598
- Address Line 1: 5615 N Main St
- City: Mishawaka
- State: Indiana
- Zip Code: 46545
- Country Name: United States
- Address: 5615 N Main St, Mishawaka, Indiana 46545, United States
- Country: United States

## Related Documents

- FDA Inspection 1311766 - Krispy Kreme Doughnut Corporation - 2026-04-07 — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2026
- FDA Inspection 1238958 - Krispy Kreme Doughnut Corporation - 2024-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2024
- [FDA Inspection 1238958 - Krispy Kreme Doughnut Corporation - 2024-05-02](https://www.keypedia.com/records/fda_inspections/krispy-kreme-doughnut-corporation/f2987f4f-ca94-496b-a53a-c509b29d00c4) — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2024
- FDA Inspection 1152556 - Krispy Kreme Doughnut Corporation - 2021-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2021
- FDA Inspection 1152556 - Krispy Kreme Doughnut Corporation - 2021-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2021
- FDA Inspection 1050219 - Krispy Kreme Doughnut Corporation - 2018-03-21 — source: FDA, date: March 21, 2018
- FDA Inspection 918658 - Krispy Kreme Doughnut Corporation - 2015-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2015
- FDA Inspection 805368 - Krispy Kreme Doughnut Corporation - 2012-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2012
- FDA Inspection 694870 - Krispy Kreme Doughnut Corporation - 2010-10-01 — classification: No Action Indicated (NAI), source: FDA, date: October 1, 2010

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