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Facility profile

Bayer AG

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Wuppertal · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed5 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) manufacturePack
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
Voluntary action indicated (VAI)

Jan 18, 2023 · FDA documented observations for voluntary correction.

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 voluntary 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 history8 inspection records

FDA inspection history

8 records, May 2009 – Jan 2023 · 6 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Jan 18, 2023VAIDrug Quality Assurance2023
Jun 29, 2018NAIDrug Quality Assurance2018
Jun 29, 2018NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2018
Apr 30, 2015NAIDrug Quality Assurance2015
Dec 6, 2012NAIDrug Quality Assurance2013
May 27, 2010VAIBioresearch Monitoring2010
Feb 5, 2010NAIDrug Quality Assurance2010
May 26, 2009NAIDrug 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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