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Facility profile

Boehringer Ingelheim Pharma GmbH and Co. KG

Testing & analysis · Drug product manufacturing · Biberach an der Riss · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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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) manufactureLabelManufacturePack
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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 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Jul 22, 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 history10 inspection records

FDA inspection history

10 records, May 2009 – Jul 2022 · 3 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
Jul 22, 2022VAIDrug Quality Assurance2022
Sep 19, 2019VAIDrug Quality AssuranceYes2019
Aug 15, 2019NAIBioresearch Monitoring2019
Apr 5, 2019VAIDrug Quality AssuranceYes2019
May 30, 2014VAIDrug Quality Assurance2014
Mar 19, 2013NAIDrug Quality Assurance2013
Mar 13, 2012VAIDrug Quality Assurance2012
May 26, 2010VAIDrug Quality Assurance2010
Jan 28, 2010NAIDrug Quality Assurance2010
May 19, 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

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