# Relish Foods, Inc. dba Gourmet Fusion Foods, El Segundo, CA – FDA Inspections

Source: https://www.keypedia.com/companies/relish-foods-inc-dba-gourmet-fusion-foods/b08e7dd5-be4e-475b-b643-36aaa62081d6

> Inspection records and compliance data for Relish Foods, Inc. dba Gourmet Fusion Foods in El Segundo, California. 6 FDA inspections on record, 1 Form 483, last inspected April 08, 2026.

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## Details

- Name: Relish Foods, Inc. dba Gourmet Fusion Foods
- FEI Number: 3004333700
- Address Line 1: 200 Center St
- City: El Segundo
- State: California
- Zip Code: 90245
- Country Name: United States
- Address: 200 Center St, El Segundo, California 90245, United States
- Country: United States

## Related Documents

- FDA Inspection 1312150 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2026-04-08 — classification: No Action Indicated (NAI), source: FDA, date: April 8, 2026
- [FDA Inspection 1196725 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2023-01-25](https://www.keypedia.com/records/fda_inspections/relish-foods-inc-dba-gourmet-fusion-foods/524c835b-93b5-4d06-9444-59f8d9cad50c) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2023
- FDA Inspection 1105475 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2019-06-10 — classification: No Action Indicated (NAI), source: FDA, date: June 10, 2019
- [FDA Inspection 1081513 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2019-02-28](https://www.keypedia.com/records/fda_inspections/relish-foods-inc-dba-gourmet-fusion-foods/197c4b02-833d-4a74-ad81-f615717434d2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 28, 2019
- FDA Inspection 1037856 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2017-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2017
- [FDA Inspection 982755 - Relish Foods, Inc. dba Gourmet Fusion Foods - 2016-08-31](https://www.keypedia.com/records/fda_inspections/relish-foods-inc-dba-gourmet-fusion-foods/eb8c4b4f-9f4f-4a83-9c0a-d0d5a6a21205) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2016

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