Seabear Company FDA Inspection Record

FEI 3019350 · Inspections, Form 483s, warning letters and import refusals

Seabear Company is an FDA-inspected facility (FEI 3019350) located in Anacortes, WA, US. RegDataLab tracks 11 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 23, 2025: No Action Indicated (NAI)
Inspections on record
11 (4 VAI, 7 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
3, latest Mar 13, 2025

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Showing the 10 most recent of 11 inspections. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 23, 2025No Action Indicated (NAI)Equipment - reference device not traceable to NIST (21 CFR 113.40(a)(1))
Dec 1, 2022No Action Indicated (NAI)Sanitation monitoring (21 CFR 123.11(b))
Critical factors - frequency measured, recorded (21 CFR 113.40(j))
Process adherence (21 CFR 108.35(c)(3)(i))
Oct 10, 2019No Action Indicated (NAI)No citations listed
Apr 10, 2018Voluntary Action Indicated (VAI)HACCP plan implementation (21 CFR 123.6(b))
Critical control points (21 CFR 123.6(c)(2))
Corrective action plan (21 CFR 123.6(c)(5))
Jun 10, 2015No Action Indicated (NAI)No citations listed
Mar 22, 2012Voluntary Action Indicated (VAI)Signed and dated (21 CFR 123.6(d))
Critical control points (21 CFR 123.6(c)(2))
Sep 21, 2011Voluntary Action Indicated (VAI)Non food-contact equipment in processing area (21 CFR 110.40(c))
Floors, walls and ceilings (21 CFR 110.20(b)(4))
Manufacturing conditions (21 CFR 110.80(b)(2))
Metal / extraneous materials (21 CFR 110.80(b)(8))
Sep 2, 2010No Action Indicated (NAI)No citations listed
Jul 7, 2010No Action Indicated (NAI)No citations listed
Sep 17, 2009No Action Indicated (NAI)No citations listed

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Mar 13, 2025Class IIF-0684-2025SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz… and 1 more product
Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Sep 8, 2021Class IIF-1009-2021Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and…
Potential for growth of C. botulinum
Apr 11, 2018Class IF-1126-2018Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz… and 1 more product
Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Seabear Company
Location
Anacortes, WA (US)
Source
inspections

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.