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TERUMO EUROPE N.V. — FDA Facility Profile

FEI 3001570557

TERUMO EUROPE N.V. is an FDA-registered facility (FEI 3001570557) located in LEUVEN Vlaams Brabant, BE. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jul 12, 2018: No Action Indicated (NAI)
Inspections on record
3 (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
4

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
Jul 12, 2018No Action Indicated (NAI)No citations listed
Jun 29, 2017No Action Indicated (NAI)No citations listed
May 30, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
Terumo Europe
Location
LEUVEN Vlaams Brabant (BE)
Source
device

Import refusals

FDA data resources

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