Labverity
Facility profile

AbbVie Deutschland GmbH & Co KG

Testing & analysis · Drug product manufacturing · Ludwigshafen · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed14 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.

AnalysisLabelManufacturePack
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
No action indicated (NAI)

May 16, 2025 · 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, May 2009 – May 2025 · 3 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
May 16, 2025NAIBioresearch Monitoring2025
Sep 28, 2023VAIDrug Quality Assurance2023
Jul 19, 2019NAIDrug Quality Assurance2019
Sep 18, 2014NAIDrug Quality Assurance2014
Oct 25, 2012VAIDrug Quality AssuranceYes2013
Dec 17, 2009VAIDrug Quality Assurance2010
May 15, 2009VAIDrug Quality Assurance2009

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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