Northeast Seafood Products, Incorporated

FDA Regulatory Profile

Northeast Seafood Products, Incorporated has 1 FDA recall (1 Class I), 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest recall
F-0158-2022 · Class I · Oct 7, 2021
Latest inspection
Oct 19, 2021 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1 (1 Class I)Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-0158-2022Class IHaddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod…Oct 7, 2021

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 19, 2021Denver, COFood/CosmeticsOfficial Action Indicated (OAI)1720694
Aug 31, 2020Denver, COFood/CosmeticsNo Action Indicated (NAI)1720694
Nov 1, 2016Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)1720694
Jun 15, 2011Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)1720694
Feb 4, 2009Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)1720694

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1720694Denver, CO5Oct 19, 2021

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