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International Marine Products Inc. Houston FDA Inspection Record

FEI 3011254064 · Inspections, Form 483s, warning letters and import refusals

International Marine Products Inc. Houston is an FDA-inspected facility (FEI 3011254064) located in Houston, TX, US. RegDataLab tracks 4 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 28, 2025: Voluntary Action Indicated (VAI)
Inspections on record
4 (2 VAI, 2 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 Nov 9, 2019

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
Mar 28, 2025Voluntary Action Indicated (VAI)HACCP plan implementation (21 CFR 123.6(b))
Jul 15, 2021No Action Indicated (NAI)No HACCP plan (21 CFR 123.6(b))
HACCP plan implementation (21 CFR 123.6(b))
Nov 25, 2019Voluntary Action Indicated (VAI)No HACCP plan (21 CFR 123.6(b))
HACCP plan implementation (21 CFR 123.6(b))
Oct 5, 2017No 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
Nov 9, 2019Class IF-0229-2020Sushi grade yellowfin tuna individually wrapped in various product weights. and 2 more products
Potential to be contaminated with Listeria monocytogenes

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 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.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIMar 28, 20256 x 16
Class I recall F-0229-2020, this FEI as the recalling firmNov 9, 201915 x 0.253.8
Inspection classified VAINov 25, 20196 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
International Marine Products Inc. Houston
Location
Houston, TX (US)
Source
inspections

FDA data resources

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