# Trident Seafoods Corporation - Inspection Records

Source: https://www.keypedia.com/companies/trident-seafoods-corporation/24679ec1-da5e-4f92-bc9d-d7323bfed679

> Inspection records and compliance data for Trident Seafoods Corporation in Seattle, Washington. Access full analysis and detailed observations.

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## Details

- Name: Trident Seafoods Corporation
- FEI Number: 1000130364
- City: Seattle
- State: Washington
- Country Name: United States
- Address Line 1: 5303 Shilshole Ave Nw
- Zip Code: 98107

## Related Documents

- [FDA Inspection 1181181 - Trident Seafoods Corporation - 2022-08-26](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/69297307-b44d-48b5-bfff-8b38106593fe) — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2022
- [FDA Inspection 1053686 - Trident Seafoods Corporation - 2018-05-07](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/01d932c4-e852-49d3-be3a-76896f59d216) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2018
- [FDA Inspection 1025077 - Trident Seafoods Corporation - 2017-08-22](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/e0ab93ec-a310-4dce-8568-587a7ecce6c4) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2017
- [FDA Inspection 874432 - Trident Seafoods Corporation - 2014-04-15](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/dba751cc-b7fd-49d0-a59d-ce56ed0ea7cb) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2014
- [FDA Inspection 727939 - Trident Seafoods Corporation - 2011-05-26](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/0ed6b147-dcdf-4a0f-81d8-a9e98f5b7cd8) — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011
- [FDA Inspection 575283 - Trident Seafoods Corporation - 2009-03-26](https://www.keypedia.com/records/fda_inspections/trident-seafoods-corporation/ec5d6f6f-63c8-462b-aa4c-87746e98bb4d) — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2009

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