International Marine Products Inc. Los Angeles FDA Inspection Record

FEI 3011067496 · Inspections, Form 483s, warning letters and import refusals

International Marine Products Inc. Los Angeles is an FDA-inspected facility (FEI 3011067496) located in Los Angeles, CA, US. RegDataLab tracks 9 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Jun 12, 2026: No Action Indicated (NAI)
Inspections on record
9 (2 OAI, 3 VAI, 4 NAI)
Last OAI inspection
Mar 22, 2017
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

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 12, 2026No Action Indicated (NAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP plan implementation (21 CFR 123.6(b))
Food safety hazards (21 CFR 123.6(c)(1))
Aug 10, 2022Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Jul 7, 2021No Action Indicated (NAI)No citations listed
Mar 22, 2017Official Action Indicated (OAI)Precautions against contamination--micro, foreign substances (21 CFR 110.10(b)(9))
Food-contact - unlawful indirect additives (21 CFR 110.40(a))
Importer verification (21 CFR 123.12(a)(2))
Oct 28, 2015Voluntary Action Indicated (VAI)No citations listed
Aug 6, 2013No Action Indicated (NAI)No citations listed
Oct 14, 2010Voluntary Action Indicated (VAI)No citations listed
Aug 24, 2010No Action Indicated (NAI)No citations listed
Jul 29, 2009Official Action Indicated (OAI)Sanitation monitoring (21 CFR 123.11(b))
Monitoring - adequacy (21 CFR 123.6(c)(4))
Verification - record review - frequency (21 CFR 123.8(a)(3))
HACCP plan implementation (21 CFR 123.6(b))
and 2 more

FDA record score

11 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 15, 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
Inspection classified OAIMar 22, 201730 x 0.257.5
Inspection classified VAIAug 10, 20226 x 0.63.6
Inspection classified VAIOct 28, 201510 years or older, so it adds no points0
Inspection classified VAIOct 14, 201010 years or older, so it adds no points0
Inspection classified OAIJul 29, 200910 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 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 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 15, 2026Newest record Nov 5, 2026Current

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Facility details

Company
International Marine Products Inc. Los Angeles
Location
Los Angeles, CA (US)
Source
inspections

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