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Mainfreight, Inc.

FDA Regulatory Profile

Mainfreight, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Mainfreight, Inc." and its spelling variant "Mainfreight".

Latest inspection
Jun 10, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA Record by Year

Mainfreight, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Mainfreight, Inc.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 1 inspections120242025: 0 inspections020252026: 2 inspections22026
YearInspectionsOAIWarning lettersRecall recordsClass I
202620000
202500000
202410000
202310000
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202000000
201900000
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Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA Inspections

4 inspections from Apr 13, 2023 to Jun 10, 2026.

DateSiteProductClassificationFEI
Jun 10, 2026Wind Gap, PAFood/CosmeticsNo Action Indicated (NAI)3020270745
Jan 12, 2026East Point, GAFood/CosmeticsNo Action Indicated (NAI)3008865455
Nov 8, 2024Flower Mound, TXFood/CosmeticsNo Action Indicated (NAI)3013025327
Apr 13, 2023Tacoma, WAFood/CosmeticsNo Action Indicated (NAI)3017407149

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

4 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3020270745Wind Gap, PA1Jun 10, 2026
FEI 3008865455East Point, GA1Jan 12, 2026
FEI 3013025327Flower Mound, TX1Nov 8, 2024
FEI 3017407149Tacoma, WA1Apr 13, 2023

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FDA data resources

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