Actavis Laboratories UT, Inc.

FDA Regulatory Profile

Actavis Laboratories UT, Inc. has 0 FDA recalls, 12 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Actavis Laboratories UT, Inc." and its spelling variant "Actavis Laboratories Ut". They do not include records filed under Teva or other names in its corporate family.

Latest inspection
Sep 19, 2025 · VAI

Part of the Teva corporate family.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections12Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Actavis Laboratories UT, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Actavis Laboratories UT, Inc.: FDA inspections per year 2017: 1 inspections120172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 1 inspections120242025: 1 inspections120252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202510000
202411000
202300000
202200000
202110000
202000000
201900000
201810000
201710000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

12 inspections from Apr 24, 2009 to Sep 19, 2025.

DateSiteProductClassificationFEI
Sep 19, 2025Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Mar 19, 2024Salt Lake City, UTDrugsOfficial Action Indicated (OAI)1000117147
Aug 20, 2021Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Aug 2, 2018Salt Lake City, UTDrugsNo Action Indicated (NAI)1000117147
Oct 25, 2017Salt Lake City, UTDrugsNo Action Indicated (NAI)1000117147
Dec 8, 2015Salt Lake City, UTDrugsNo Action Indicated (NAI)1000117147
Oct 17, 2014Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Jan 17, 2014Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Dec 14, 2012Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Jun 8, 2012Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Jan 14, 2011Salt Lake City, UTDrugsVoluntary Action Indicated (VAI)1000117147
Apr 24, 2009Salt Lake City, UTDrugsNo Action Indicated (NAI)1000117147
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1000117147Salt Lake City, UT12Sep 19, 2025

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