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Facility profile

Bayer Weimar GmbH und Co. KG

Testing & analysis · Drug product manufacturing · Weimar · Germany

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed
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.

AnalysisManufacture
Due diligence

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
Voluntary action indicated (VAI)

Nov 24, 2022 · 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 history5 inspection records

FDA inspection history

5 records, Dec 2009 – Nov 2022 · 2 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 24, 2022VAIDrug Quality Assurance2023
Sep 13, 2019VAIDrug Quality AssuranceYes2019
Nov 5, 2015NAIDrug Quality Assurance2016
Oct 19, 2012NAIDrug Quality Assurance2013
Dec 4, 2009VAIDrug Quality Assurance2010

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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