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Facility profile

HOVIONE LIMITED

Testing & analysis · Drug product manufacturing · CORK P43 DY23 · Ireland

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed4 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisActive pharmaceutical ingredient (API) manufactureManufacture
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Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 22, 2026

Latest matched inspection
No action indicated (NAI)

Jan 20, 2023 · No conditions warranted FDA action in this inspection.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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Shows

Registration status and a latest matched no action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history7 inspection records

FDA inspection history

7 records, Mar 2012 – Jan 2023 · 3 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Jan 20, 2023NAIDrug Quality Assurance2023
Feb 22, 2022VAIDrug Quality Assurance2022
Dec 22, 2017NAIDrug Quality Assurance2018
Jul 25, 2014NAIDrug Quality Assurance2014
Mar 16, 2012VAIDrug Quality Assurance2012
Mar 16, 2012VAIPre-Approval Eval. of Animal Drugs and Food Additives2012
Mar 16, 2012VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2012

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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