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Boehringer Ingelheim RCV GmbH & Co KG

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Austria A1121 · Austria

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) manufacture
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)

Nov 12, 2024 · 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.

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Method and source details
View full inspection and compliance history9 inspection records

FDA inspection history

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

DateClassProject areaCitationsFY
Nov 12, 2024NAIVaccines and Allergenic Products2025
Mar 2, 2023NAIDrug Quality Assurance2023
Sep 16, 2022NAIVaccines and Allergenic Products2022
Jan 28, 2021VAIDrug Quality Assurance2021
Nov 11, 2014VAIDrug Quality Assurance2015
Nov 15, 2013NAIDrug Quality Assurance2014
Apr 26, 2013VAIDrug Quality Assurance2013
Mar 23, 2012VAIDrug Quality Assurance2012
Jan 28, 2010VAIDrug 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

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