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Lucullus SAS

FDA Regulatory Profile

Lucullus SAS has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Lucullus SAS" and its spelling variant "Lucullus".

Latest inspection
Feb 27, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

2 inspections from Feb 24, 2025 to Feb 27, 2025.

DateSiteProductClassificationFEI
Feb 27, 2025Prouvy, FranceFood/CosmeticsNo Action Indicated (NAI)3021630835
Feb 24, 2025Le Touquet-Paris-Plage, FranceFood/CosmeticsNo Action Indicated (NAI)3030651562

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3021630835Prouvy, France1Feb 27, 2025
FEI 3030651562Le Touquet-Paris-Plage, France1Feb 24, 2025

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FDA data resources

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