Mylan Teoranta

FDA Regulatory Profile

Mylan Teoranta has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 15, 2022 · VAI

Newer recall under related name Viatris: Oct 1, 2026, D-0049-2027.

Part of the Viatris corporate family.

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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
Inspections7Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Viatris
parent company
260211Oct 1, 2026 (D-0049-2027)
Mylan Institutional
Same company group
24000Mar 7, 2025 (D-0291-2025)
Mylan
Same company group
5000Dec 20, 2016 (D-0444-2017)
Meda Pharmaceuticals
Same company group
10101Oct 17, 2011 (D-1418-2012)
Mylan Laboratories Limited
Same company group
00334—
Dpt Laboratories
Same company group
03240—
Viatris Pharmaceuticals
Same company group
00180—
Mylan Technologies
Same company group
0070—
Mylan Laboratories
Same company group
0010—

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 15, 2022Inverin, IrelandDrugsVoluntary Action Indicated (VAI)3002806521
Jun 22, 2018Inverin, IrelandDrugsVoluntary Action Indicated (VAI)3002806521
Feb 16, 2018Inverin, IrelandDrugsVoluntary Action Indicated (VAI)3002806521
Jun 15, 2016Inverin, IrelandDrugsNo Action Indicated (NAI)3002806521
May 27, 2014Inverin, IrelandDrugsVoluntary Action Indicated (VAI)3002806521
Mar 30, 2012Inverin, IrelandDrugsNo Action Indicated (NAI)3002806521
Oct 15, 2009Inverin, IrelandDrugsNo Action Indicated (NAI)3002806521

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 3002806521Inverin, Ireland7Jul 15, 2022

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