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Facility profile

Catalent Germany Schorndorf GmbH

Testing & analysis · Drug product manufacturing · Schorndorf · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed23 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.

AnalysisLabelManufacturePack
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)

Mar 17, 2022 · 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 history7 inspection records

FDA inspection history

7 records, Sep 2009 – Mar 2022 · 2 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Mar 17, 2022VAIDrug Quality Assurance2022
Feb 14, 2020VAIDrug Quality Assurance2020
Sep 21, 2018VAIDrug Quality AssuranceYes2018
Oct 26, 2016VAIDrug Quality Assurance2017
Feb 7, 2014NAIDrug Quality Assurance2014
Feb 10, 2012NAIDrug Quality Assurance2012
Sep 3, 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

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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