# Pacific Seafood - Newport, LLC (East Plant), Newport, OR – FDA Inspections

Source: https://www.keypedia.com/companies/pacific-seafood-newport-llc-east-plant/e41d15ea-2a50-4a3d-8dee-fcb8851b2829

> Inspection records and compliance data for Pacific Seafood - Newport, LLC (East Plant) in Newport, Oregon. 7 FDA inspections on record, 1 Form 483, last inspected August 07, 2024.

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## Details

- Name: Pacific Seafood - Newport, LLC (East Plant)
- FEI Number: 3020949
- Address Line 1: 213 Sw Bay Blvd
- City: Newport
- State: Oregon
- Zip Code: 97365
- Country Name: United States
- Address: 213 Sw Bay Blvd, Newport, Oregon 97365, United States
- Country: United States

## Related Documents

- FDA Inspection 1245229 - Pacific Seafood - Newport, LLC (East Plant) - 2024-08-07 — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2024
- FDA Inspection 1155193 - Pacific Seafood - Newport, LLC (East Plant) - 2021-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2021
- [FDA Inspection 1059613 - Pacific Seafood - Newport, LLC (East Plant) - 2018-07-19](https://www.keypedia.com/records/fda_inspections/pacific-seafood-newport-llc-east-plant/65fe93b8-3a29-4e66-88ab-25b4d2d05f5a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 19, 2018
- [FDA Inspection 935233 - Pacific Seafood - Newport, LLC (East Plant) - 2015-07-22](https://www.keypedia.com/records/fda_inspections/pacific-seafood-newport-llc-east-plant/ce89d906-6525-4d0b-8c8b-ec204fc60392) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 22, 2015
- FDA Inspection 762339 - Pacific Seafood - Newport, LLC (East Plant) - 2012-01-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2012
- FDA Inspection 635481 - Pacific Seafood - Newport, LLC (East Plant) - 2009-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2009
- FDA Inspection 597545 - Pacific Seafood - Newport, LLC (East Plant) - 2009-05-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 22, 2009

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