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AL DENTE PASTA

FDA Regulatory Profile

AL DENTE PASTA has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 16, 2025 · 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 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 16, 2025Whitmore Lake, MIFood/CosmeticsNo Action Indicated (NAI)3027613512
Mar 19, 2014Saginaw, MIFood/CosmeticsVoluntary Action Indicated (VAI)1833259
Apr 17, 2012Saginaw, MIFood/CosmeticsNo Action Indicated (NAI)1833259

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 3027613512Whitmore Lake, MI1Sep 16, 2025
FEI 1833259Saginaw, MI2Mar 19, 2014

FDA data resources

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