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Median Technologies — FDA Facility Profile

FEI 3005312556

Median Technologies is an FDA-inspected facility (FEI 3005312556) located in Valbonne, FR. RegDataLab tracks 6 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jul 17, 2026: No Action Indicated (NAI)
Inspections on record
6 (6 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
Jul 17, 2026No Action Indicated (NAI)No citations listed
May 16, 2024No Action Indicated (NAI)No citations listed
Jul 20, 2023No Action Indicated (NAI)No citations listed
Nov 12, 2021No Action Indicated (NAI)No citations listed
May 3, 2019No Action Indicated (NAI)No citations listed
Jan 12, 2017No Action Indicated (NAI)No citations listed

Facility details

Company
Median Technologies
Location
Valbonne (FR)
Source
inspections

FDA data resources

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