# Daylight Donut Flour Co. LLC, Tulsa, OK – FDA Inspections

Source: https://www.keypedia.com/companies/daylight-donut-flour-co-llc/e000d0dd-9065-46dd-9369-086974934b06

> Inspection records and compliance data for Daylight Donut Flour Co. LLC in Tulsa, Oklahoma. 7 FDA inspections on record, last inspected September 17, 2026.

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## Details

- Name: Daylight Donut Flour Co. LLC
- FEI Number: 1627915
- Address Line 1: 11707 E 11th St
- City: Tulsa
- State: Oklahoma
- Zip Code: 74128
- Country Name: United States
- Address: 11707 E 11th St, Tulsa, Oklahoma 74128, United States
- Country: United States

## Related Documents

- FDA Inspection 1337310 - Daylight Donut Flour Co. LLC - 2026-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2026
- FDA Inspection 1267222 - Daylight Donut Flour Co. LLC - 2025-03-18 — source: FDA, date: March 18, 2025
- FDA Inspection 1267222 - Daylight Donut Flour Co. LLC - 2025-03-18 — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2025
- FDA Inspection 1267222 - Daylight Donut Flour Co. LLC - 2025-03-18 — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2025
- FDA Inspection 1156699 - Daylight Donut Flour Co. LLC - 2021-11-09 — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2021
- FDA Inspection 1156699 - Daylight Donut Flour Co. LLC - 2021-11-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 9, 2021
- FDA Inspection 1039394 - Daylight Donut Flour Co. LLC - 2017-12-22 — classification: No Action Indicated (NAI), source: FDA, date: December 22, 2017
- FDA Inspection 909184 - Daylight Donut Flour Co. LLC - 2014-12-18 — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- FDA Inspection 827812 - Daylight Donut Flour Co. LLC - 2013-04-17 — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2013
- FDA Inspection 827812 - Daylight Donut Flour Co. LLC - 2013-04-17 — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2013

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