Veranova LP

FDA Regulatory Profile

Veranova LP has 0 FDA recalls, 14 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 23, 2026 · 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
Inspections14Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 23, 2026West Deptford, NJDrugsVoluntary Action Indicated (VAI)2245277
Jul 31, 2025Devens, MADrugsNo Action Indicated (NAI)2018076
Feb 15, 2023West Deptford, NJDrugsVoluntary Action Indicated (VAI)2245277
Mar 8, 2019West Deptford, NJDrugsVoluntary Action Indicated (VAI)2245277
Jan 31, 2019Devens, MADrugsNo Action Indicated (NAI)2018076
Jan 31, 2018West Deptford, NJVeterinaryVoluntary Action Indicated (VAI)2245277
Sep 2, 2016Devens, MADrugsVoluntary Action Indicated (VAI)2018076
May 5, 2016West Deptford, NJDrugsNo Action Indicated (NAI)2245277
Dec 2, 2013Devens, MADrugsNo Action Indicated (NAI)2018076
Oct 31, 2013West Deptford, NJVeterinaryNo Action Indicated (NAI)2245277
Jun 21, 2012West Deptford, NJVeterinaryNo Action Indicated (NAI)2245277
Nov 7, 2011Devens, MADrugsVoluntary Action Indicated (VAI)2018076
Jun 11, 2010West Deptford, NJDrugsNo Action Indicated (NAI)2245277
Feb 26, 2010Devens, MAVeterinaryNo Action Indicated (NAI)2018076

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 2245277West Deptford, NJ8Jan 23, 2026
FEI 2018076Devens, MA6Jul 31, 2025

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