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HARBOR MARINE PRODUCT INC FDA Inspection Record

FEI 3007556381 · Inspections, Form 483s, warning letters and import refusals

HARBOR MARINE PRODUCT INC is an FDA-inspected facility (FEI 3007556381) located in Vernon, CA, US. RegDataLab tracks 3 FDA inspections and 2 compliance actions at this facility.

What FDA found at this site

Latest inspection
Jun 1, 2026: Voluntary Action Indicated (VAI)
Inspections on record
3 (1 OAI, 2 VAI)
Last OAI inspection
Mar 27, 2025
Warning letters
2 listed by FDA for this FEI, latest Dec 1, 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

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Jun 1, 2026Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP training or qualification (21 CFR 123.10)
HACCP plan implementation (21 CFR 123.6(b))
Signed and dated (21 CFR 123.6(d))
and 1 more
Mar 27, 2025Official Action Indicated (OAI)Sanitation monitoring (21 CFR 123.11(b))
Qualifications of individuals (21 CFR 117.4)
HACCP plan implementation (21 CFR 123.6(b))
Importer verification (21 CFR 123.12(a)(2))
and 1 more
Feb 12, 2020Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP plan implementation (21 CFR 123.6(b))
Importer verification (21 CFR 123.12(a)(2))
Food safety hazards (21 CFR 123.6(c)(1))
and 2 more

FDA record score

75 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

5 records behind this number
RecordDatePoints x age weightAdds
Warning letter, no close-out letter listedDec 1, 202530 x 130
Inspection classified OAIMar 27, 202530 x 130
Warning letter on FDA's dashboard, which does not show close-outsMay 8, 201730 x 0.257.5
Inspection classified VAIJun 1, 20266 x 16
Inspection classified VAIFeb 12, 20206 x 0.251.5

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
HARBOR MARINE PRODUCT, INC.
Location
Vernon, CA (US)
Source
inspections

Compliance actions

FDA data resources

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