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Jan De Bleecker, MD., CI — FDA Facility Profile

FEI 3013184718

Jan De Bleecker, MD., CI is an FDA-inspected facility (FEI 3013184718) located in Gent, BE. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 11, 2017: Voluntary Action Indicated (VAI)
Inspections on record
2 (1 VAI, 1 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

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
May 11, 2017Voluntary Action Indicated (VAI)No citations listed
Feb 23, 2017No Action Indicated (NAI)No citations listed

Facility details

Company
Jan De Bleecker, MD., CI
Location
Gent (BE)
Source
inspections

FDA data resources

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