F. Alioto Company, Inc.

FDA Regulatory Profile

F. Alioto Company, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 1, 2025 · VAI

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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
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 1, 2025San Francisco, CAFood/CosmeticsVoluntary Action Indicated (VAI)2916513
Jul 27, 2022San Francisco, CAFood/CosmeticsVoluntary Action Indicated (VAI)2916513
Dec 19, 2017San Francisco, CAFood/CosmeticsNo Action Indicated (NAI)2916513
Jan 14, 2015San Francisco, CAFood/CosmeticsVoluntary Action Indicated (VAI)2916513
Jun 21, 2012San Francisco, CAFood/CosmeticsNo Action Indicated (NAI)2916513
Nov 18, 2009San Francisco, CAFood/CosmeticsNo Action Indicated (NAI)2916513

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 2916513San Francisco, CA6Jul 1, 2025

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