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Haydel Enterprises Inc

FDA Regulatory Profile

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

Latest inspection
Nov 14, 2019 · 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
Inspections4Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 14, 2019Jefferson, LAFood/CosmeticsVoluntary Action Indicated (VAI)2317331
Sep 21, 2017Jefferson, LAFood/CosmeticsNo Action Indicated (NAI)2317331
Oct 1, 2014Jefferson, LAFood/CosmeticsNo Action Indicated (NAI)2317331
Apr 3, 2012Jefferson, LAFood/CosmeticsNo Action Indicated (NAI)2317331

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 2317331Jefferson, LA4Nov 14, 2019

FDA data resources

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