Labverity
Facility profile

Simtra Deutschland GmbH

Testing & analysis · Drug product manufacturing · Halle/Westfalen · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 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) manufactureLabelManufacturePackParticle Size ReductionSterilize
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
Official action indicated (OAI)

Sep 26, 2025 · The findings may warrant official FDA action.

Matched compliance actions
Warning Letter · Mar 2026

Within five years · review the action and follow-up.

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Shows

Registration status and a latest matched official 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 history11 inspection records

FDA inspection history

11 records, Jul 2010 – Sep 2025 · 6 NAI · 4 VAI · 1 OAI

DateClassProject areaCitationsFY
Sep 26, 2025OAIDrug Quality AssuranceYes2025
May 3, 2023NAIDrug Quality Assurance2023
Jan 29, 2020VAIDrug Quality Assurance2020
Sep 3, 2019NAIDrug Quality Assurance2019
Jun 14, 2018VAIDrug Quality Assurance2018
Jun 27, 2017VAIDrug Quality Assurance2017
Mar 18, 2016VAIDrug Quality AssuranceYes2016
Jul 1, 2014NAIDrug Quality Assurance2014
Jul 20, 2013NAIDrug Quality Assurance2013
Aug 26, 2011NAIDrug Quality Assurance2011
Jul 22, 2010NAIDrug Quality Assurance2010

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Mar 3, 2026Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

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