# Dawn Food Products Inc, Louisville, KY – FDA Inspections

Source: https://www.keypedia.com/companies/dawn-food-products-inc/df0d4f55-0e53-476b-85b5-7470219b161d

> Inspection records and compliance data for Dawn Food Products Inc in Louisville, Kentucky. 5 FDA inspections on record, last inspected December 14, 2023.

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## Details

- Name: Dawn Food Products Inc
- FEI Number: 1021813
- Address Line 1: 6303 Kenjoy Dr
- City: Louisville
- State: Kentucky
- Zip Code: 40214
- Country Name: United States
- Address: 6303 Kenjoy Dr, Louisville, Kentucky 40214, United States
- Country: United States

## Related Documents

- FDA Inspection 1227857 - Dawn Food Products Inc - 2023-12-14 — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2023
- FDA Inspection 1009404 - Dawn Food Products Inc - 2017-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- [FDA Inspection 1009404 - Dawn Food Products Inc - 2017-04-13](https://www.keypedia.com/records/fda_inspections/dawn-food-products-inc/c1d66e73-4992-4f38-8eaa-43d86052c54c) — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- FDA Inspection 1009404 - Dawn Food Products Inc - 2017-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- FDA Inspection 1009404 - Dawn Food Products Inc - 2017-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- FDA Inspection 846354 - Dawn Food Products Inc - 2013-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- FDA Inspection 665842 - Dawn Food Products Inc - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- FDA Inspection 665842 - Dawn Food Products Inc - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- FDA Inspection 665842 - Dawn Food Products Inc - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- FDA Inspection 665842 - Dawn Food Products Inc - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010

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