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Facility profile

Bayer AG

Testing & analysis · Drug product manufacturing · Berlin · 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) manufactureLabelManufacturePackSterilize
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Jun 6, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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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 history9 inspection records

FDA inspection history

9 records, Nov 2010 – Jun 2024 · 4 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Jun 6, 2024VAIDrug Quality Assurance2024
Aug 27, 2021VAIDrug Quality Assurance2021
Sep 24, 2019VAIDrug Quality AssuranceYes2019
Jan 24, 2017NAIDrug Quality Assurance2017
May 13, 2014VAIDrug Quality AssuranceYes2014
Apr 17, 2014NAIBioresearch Monitoring2014
Sep 18, 2012VAIDrug Quality Assurance2012
Nov 19, 2010NAIDrug Quality Assurance2011
Nov 16, 2010NAIBioresearch Monitoring2011

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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