Swabplus, L.P.

FDA Regulatory Profile

Swabplus, L.P. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 1, 2023 · OAI

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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
Inspections8Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 1, 2023Rancho Cucamonga, CADrugsOfficial Action Indicated (OAI)3003053677
Oct 15, 2021Rancho Cucamonga, CADrugsOfficial Action Indicated (OAI)3003053677
Apr 11, 2019Rancho Cucamonga, CAVeterinaryNo Action Indicated (NAI)3003053677
Jun 30, 2016Rancho Cucamonga, CADrugsVoluntary Action Indicated (VAI)3003053677
Mar 28, 2014Rancho Cucamonga, CAVeterinaryNo Action Indicated (NAI)3003053677
Jul 21, 2011Rancho Cucamonga, CADrugsVoluntary Action Indicated (VAI)3003053677
Jun 9, 2010Rancho Cucamonga, CADrugsNo Action Indicated (NAI)3003053677
Nov 25, 2008Rancho Cucamonga, CAFood/CosmeticsNo Action Indicated (NAI)3003053677

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 3003053677Rancho Cucamonga, CA8Aug 1, 2023

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