Takeda GmbH — FDA Facility Profile

FEI 3002806542

Takeda GmbH is an FDA-registered facility (FEI 3002806542) located in Baden-Wurttemberg, DE. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 7 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Nov 12, 2025: Voluntary Action Indicated (VAI)
Inspections on record
7 (4 VAI, 3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
5

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Nov 12, 2025Voluntary Action Indicated (VAI)No citations listed
May 6, 2021Voluntary Action Indicated (VAI)No citations listed
Mar 27, 2018No Action Indicated (NAI)No citations listed
Apr 22, 2016No Action Indicated (NAI)No citations listed
Feb 21, 2014No Action Indicated (NAI)No citations listed
Apr 27, 2012Voluntary Action Indicated (VAI)No citations listed
Jun 10, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Takeda GmbH
Location
Baden-Wurttemberg (DE)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.