# Bornstein Seafoods Inc, Bellingham, WA – FDA Inspections

Source: https://www.keypedia.com/companies/bornstein-seafoods-inc/7d321180-4254-4b26-8c34-7fe67dcf487f

> Inspection records and compliance data for Bornstein Seafoods Inc in Bellingham, Washington. 7 FDA inspections on record, last inspected March 21, 2023.

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## Details

- Name: Bornstein Seafoods Inc
- FEI Number: 3011041
- Address Line 1: 1001 Hilton Ave
- City: Bellingham
- State: Washington
- Zip Code: 98225
- Country Name: United States
- Address: 1001 Hilton Ave, Bellingham, Washington 98225, United States
- Country: United States

## Related Documents

- FDA Inspection 1201677 - Bornstein Seafoods Inc - 2023-03-21 — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2023
- FDA Inspection 1201677 - Bornstein Seafoods Inc - 2023-03-21 — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2023
- FDA Inspection 1106957 - Bornstein Seafoods Inc - 2019-05-07 — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2019
- FDA Inspection 1097915 - Bornstein Seafoods Inc - 2019-05-07 — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2019
- [FDA Inspection 977400 - Bornstein Seafoods Inc - 2016-06-24](https://www.keypedia.com/records/fda_inspections/bornstein-seafoods-inc/e61ee702-d14e-4f15-be6b-96b775311aee) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2016
- [FDA Inspection 885538 - Bornstein Seafoods Inc - 2014-06-27](https://www.keypedia.com/records/fda_inspections/bornstein-seafoods-inc/38bfc8ce-2edd-4a36-86eb-616d8d2d0382) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 27, 2014
- [FDA Inspection 760633 - Bornstein Seafoods Inc - 2011-12-30](https://www.keypedia.com/records/fda_inspections/bornstein-seafoods-inc/018e16a9-d3f7-4849-92b8-665de25d7919) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 30, 2011
- FDA Inspection 657999 - Bornstein Seafoods Inc - 2010-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2010

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