Bon Appetit Danish, Inc.

FDA Regulatory Profile

Bon Appetit Danish, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 17, 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
Inspections6Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2025Vernon, CAFood/CosmeticsNo Action Indicated (NAI)3014277797
Jun 26, 2025Vernon, CAFood/CosmeticsNo Action Indicated (NAI)3009590274
Apr 18, 2023Vernon, CAVeterinaryNo Action Indicated (NAI)2026137
Sep 27, 2022Vernon, CAVeterinaryNo Action Indicated (NAI)3009590274
Oct 16, 2019Vernon, CAFood/CosmeticsNo Action Indicated (NAI)2026137
Jan 30, 2014Vernon, CAFood/CosmeticsNo Action Indicated (NAI)2026137

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 3014277797Vernon, CA1Jul 17, 2025
FEI 3009590274Vernon, CA2Jun 26, 2025
FEI 2026137Vernon, CA3Apr 18, 2023

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