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Lonza Tampa LLC

FDA Regulatory Profile

Lonza Tampa LLC has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 22, 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 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 22, 2025Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109
Sep 29, 2023Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109
Oct 1, 2021Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109
Jul 20, 2018Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109
Jul 14, 2017Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109
Dec 10, 2008Tampa, FLDrugsVoluntary Action Indicated (VAI)3001549109

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 3001549109Tampa, FL6Aug 22, 2025

FDA data resources

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