# Seattle Gourmet Foods LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/seattle-gourmet-foods-llc/ac7762f0-6e2b-4af8-b4d3-19b846e45492

> Inspection records and compliance data for Seattle Gourmet Foods LLC in Kent, Washington. Access full analysis and detailed observations.

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## Details

- Name: Seattle Gourmet Foods LLC
- FEI Number: 3021453
- City: Kent
- State: Washington
- Country Name: United States
- Address Line 1: 19016 72nd Ave S
- Zip Code: 98032

## Related Documents

- [FDA Inspection 1281435 - Seattle Gourmet Foods LLC - 2025-04-01](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/b6e40b8c-25bb-4089-9b37-3b00924a031e) — source: FDA, date: April 1, 2025
- [FDA Inspection 1020958 - Seattle Gourmet Foods LLC - 2017-08-09](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/57aea03f-c3de-48b0-8fd5-ba9404db1e19) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 9, 2017
- [FDA Inspection 732415 - Seattle Gourmet Foods LLC - 2011-06-29](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/b2a10b5e-ada6-452d-836d-410d6094534c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- [FDA Inspection 656311 - Seattle Gourmet Foods LLC - 2010-04-13](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/9bffbcd0-b7c2-4a85-b599-74181ed29f7e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2010
- [FDA Inspection 626857 - Seattle Gourmet Foods LLC - 2009-11-05](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/95497efc-76c0-4114-9eb4-4f5c5fbbc842) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2009
- [FDA Inspection 547746 - Seattle Gourmet Foods LLC - 2008-11-20](https://www.globalkeysolutions.net/records/fda_inspections/seattle-gourmet-foods-llc/71d7a790-a627-4dd9-94bb-328450dab6fd) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2008

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