Provimi North America, Inc.

FDA Regulatory Profile

Provimi North America, Inc. has 0 FDA recalls, 22 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 25, 2024 · NAI

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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
Inspections22Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 25, 2024Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466
Mar 25, 2022Fremont, NEVeterinaryNo Action Indicated (NAI)1921541
Mar 25, 2022Fremont, NEVeterinaryNo Action Indicated (NAI)3008443810
Nov 7, 2019Fremont, NEVeterinaryNo Action Indicated (NAI)1921541
Jul 2, 2019Weatherford, TXVeterinaryNo Action Indicated (NAI)1000516203
Apr 9, 2019Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466
Mar 8, 2019Fremont, NEVeterinaryOfficial Action Indicated (OAI)1921541
Mar 8, 2019Fremont, NEVeterinaryNo Action Indicated (NAI)3008443810
Aug 29, 2018Fremont, NEVeterinaryNo Action Indicated (NAI)3008443810
Aug 29, 2018Fremont, NEVeterinaryNo Action Indicated (NAI)1921541
Aug 7, 2017Fremont, NEVeterinaryVoluntary Action Indicated (VAI)1921541
Aug 7, 2017Fremont, NEVeterinaryNo Action Indicated (NAI)3008443810
Sep 9, 2015Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466
Sep 9, 2015Fremont, NEVeterinaryVoluntary Action Indicated (VAI)1921541
May 15, 2015Weatherford, TXVeterinaryNo Action Indicated (NAI)1000516203
Dec 19, 2013Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466
May 28, 2013Fremont, NEVeterinaryNo Action Indicated (NAI)1921541
Dec 20, 2011Weatherford, TXVeterinaryNo Action Indicated (NAI)1000516203
Oct 19, 2011Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466
Mar 21, 2011Lewisburg, OHVeterinaryNo Action Indicated (NAI)1910466

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 1910466Lewisburg, OH8Nov 25, 2024
FEI 1921541Fremont, NE7Mar 25, 2022
FEI 3008443810Fremont, NE4Mar 25, 2022
FEI 1000516203Weatherford, TX3Jul 2, 2019

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