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Tubilux Pharma Spa

FDA Regulatory Profile

Tubilux Pharma Spa has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jun 14, 2024 · 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 actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 14, 2024Pomezia, ItalyDrugsVoluntary Action Indicated (VAI)3003854110
Dec 10, 2019Pomezia, ItalyDrugsVoluntary Action Indicated (VAI)3003854110
Apr 6, 2018Pomezia, ItalyDrugsOfficial Action Indicated (OAI)3003854110
Dec 9, 2016Pomezia, ItalyDrugsOfficial Action Indicated (OAI)3003854110

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 3003854110Pomezia, Italy4Jun 14, 2024

FDA data resources

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