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Northern Food I/E Inc. FDA Inspection Record

FEI 3005313357 · Inspections, Form 483s, warning letters and import refusals

Northern Food I/E Inc. is an FDA-inspected facility (FEI 3005313357) located in Westbury, NY, US. RegDataLab tracks 3 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 28, 2025: No Action Indicated (NAI)
Inspections on record
3 (2 VAI, 1 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
3, latest Dec 5, 2022

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, 2025No Action Indicated (NAI)No citations listed
May 8, 2024Voluntary Action Indicated (VAI)Personnel (21 CFR 117.10)
Sanitary operations - Plant maintenance (21 CFR 117.35(a))
Pest control (21 CFR 117.35(c))
Sanitation of food-contact surfaces - Frequency (21 CFR 117.35(d))
and 1 more
Oct 31, 2023Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Record - English (21 CFR 1.512(b)(5)(ii)(A))

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
Dec 5, 2022Class IF-0212-2023"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name…
Product contains undeclared sulfites (17.9mg/serving).
Dec 5, 2022Class IIF-0255-2023Beijing Hawthorne Candy
Product contains undeclared sulfites (7.32 mg/serving)
Apr 29, 2010Class IF-0214-2011HAVISTA brand WHITE FUNGUS, NET WT: 100g, Product of China, UPC 7 54351 19702 4 -- Firm on…
The product contained undeclared sulfites (4979 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.

FDA record score

19 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
Class I recall F-0212-2023, this FEI as the recalling firmDec 5, 202215 x 0.69
Inspection classified VAIMay 8, 20246 x 0.63.6
Inspection classified VAIOct 31, 20236 x 0.63.6
Class II recall F-0255-2023, this FEI as the recalling firmDec 5, 20224 x 0.62.4
Class I recall F-0214-2011, this FEI as the recalling firmApr 29, 201010 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 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
Northern Food I/E Inc.
Location
Westbury, NY (US)
Source
inspections

FDA data resources

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