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Leeann Chin, Inc FDA Inspection Record

FEI 3002712252 · Inspections, Form 483s, warning letters and import refusals

Leeann Chin, Inc is an FDA-inspected facility (FEI 3002712252) located in Burnsville, MN, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 24, 2025: Voluntary Action Indicated (VAI)
Inspections on record
7 (7 VAI)
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 Jun 22, 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 24, 2025Voluntary Action Indicated (VAI)Equipment and utensils - Design and maintenance (21 CFR 117.40)
Dec 16, 2019Voluntary Action Indicated (VAI)Personnel (21 CFR 117.10)
Sanitary operations - Plant sanitation (21 CFR 117.35(a))
Plant operations - Precautions (21 CFR 117.80(a))
Hazard Analysis - Identification of Hazard (21 CFR 117.130(a)(1))
and 2 more
Nov 20, 2018Voluntary Action Indicated (VAI)Personnel (21 CFR 117.10)
Plant construction and design (21 CFR 117.20(b))
Sanitary operations - Plant sanitation (21 CFR 117.35(a))
Plant operations - Precautions (21 CFR 117.80(a))
Jun 11, 2015Voluntary Action Indicated (VAI)Contamination with microorganisms, chemicals, filth, etc. (21 CFR 110.20(b)(2))
Code - required elements (21 CFR 114.80(b))
Mar 18, 2014Voluntary Action Indicated (VAI)Maintenance of equip., utensils, and finished food packaging (21 CFR 110.80(b)(1))
Code - required elements (21 CFR 114.80(b))
Inspection of containers and carriers upon receipt (21 CFR 110.80(a)(1))
Aug 23, 2011Voluntary Action Indicated (VAI)Q.C. instrument accuracy, maintenance (21 CFR 110.40(f))
Fans/air blowing equipment (21 CFR 110.20(b)(6))
Buildings/good repair (21 CFR 110.35(a))
Manufacturing conditions (21 CFR 110.80(b)(2))
and 3 more
May 3, 2010Voluntary Action Indicated (VAI)Buildings/good repair (21 CFR 110.35(a))
Manufacturing conditions (21 CFR 110.80(b)(2))
Quality control procedures (21 CFR 114.80(a))
Scheduled process (21 CFR 114.80(a)(1))
and 7 more

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
Jun 22, 2022Class IIIF-1509-2022Lee Ann Chin Thai Peanut Sauce. In glass botle. Net Wt 13.5 oz (384g) UPC 61248 87100…
Sauce found to have a pH higher than specifications.

FDA record score

9 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.

7 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIMar 24, 20256 x 16
Inspection classified VAIDec 16, 20196 x 0.251.5
Inspection classified VAINov 20, 20186 x 0.251.5
Inspection classified VAIJun 11, 201510 years or older, so it adds no points0
Inspection classified VAIMar 18, 201410 years or older, so it adds no points0
Inspection classified VAIAug 23, 201110 years or older, so it adds no points0
Inspection classified VAIMay 3, 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
Leeann Chin, Inc
Location
Burnsville, MN (US)
Source
inspections

FDA data resources

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