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Dr. Andre Vertruyen — FDA Facility Profile

FEI 3008802023

Dr. Andre Vertruyen is an FDA-inspected facility (FEI 3008802023) located in Antwerp, BE. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Apr 7, 2011: Official Action Indicated (OAI)
Inspections on record
1 (1 OAI)
Last OAI inspection
Apr 7, 2011
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

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
Apr 7, 2011Official Action Indicated (OAI)Foreign clinical trials (21 CFR 312.120(c))

Facility details

Company
Dr. Andre Vertruyen
Location
Antwerp (BE)
Source
inspections

FDA data resources

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