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Fortune Minnesota LLC FDA Inspection Record

FEI 2130144 · Inspections, Form 483s, warning letters and import refusals

Fortune Minnesota LLC is an FDA-inspected facility (FEI 2130144) located in Minneapolis, MN, US. RegDataLab tracks 13 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 17, 2026: Voluntary Action Indicated (VAI)
Inspections on record
13 (8 VAI, 5 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
1, latest May 19, 2006

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 13 inspections. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 17, 2026Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
Sanitary operations - Plant maintenance (21 CFR 117.35(a))
Corrective action per regulation (21 CFR 123.7(c))
Jun 1, 2023No Action Indicated (NAI)No citations listed
Feb 21, 2020Voluntary Action Indicated (VAI)No citations listed
Dec 21, 2018Voluntary Action Indicated (VAI)HACCP plan implementation (21 CFR 123.6(b))
Dec 22, 2015Voluntary Action Indicated (VAI)Monitoring - adequacy (21 CFR 123.6(c)(4))
No HACCP plan (21 CFR 123.6(b))
Feb 5, 2015Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP training or qualification (21 CFR 123.10)
No HACCP plan (21 CFR 123.6(b))
Nov 5, 2013No Action Indicated (NAI)No citations listed
Apr 22, 2013Voluntary Action Indicated (VAI)No citations listed
Jul 11, 2012No Action Indicated (NAI)No citations listed
May 19, 2011No 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
May 19, 2006Class IIF-359-6raw refrigerated Escolar fillets. Firm had received headed and gutted frozen Escolar…
Product contained high levels of histamine and was associated with illnesses.

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
Fortune Minnesota LLC
Location
Minneapolis, MN (US)
Source
inspections

FDA data resources

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