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Handy Wholesale Products Inc

FDA Regulatory Profile

Handy Wholesale Products Inc has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 17, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 17, 2026Salt Lake City, UTFood/CosmeticsNo Action Indicated (NAI)3006777332
Sep 5, 2025Rupert, IDFood/CosmeticsNo Action Indicated (NAI)3008300971
Jul 12, 2023Meridian, IDFood/CosmeticsNo Action Indicated (NAI)3010530335

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3006777332Salt Lake City, UT1Sep 17, 2026
FEI 3008300971Rupert, ID1Sep 5, 2025
FEI 3010530335Meridian, ID1Jul 12, 2023

FDA data resources

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