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FDA Inspection 1242707 — Median Technologies

Median Technologies — FEI 3005312556

The FDA completed an inspection of Median Technologies on May 16, 2024 in Valbonne. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 16, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Valbonne (France)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1211363 (NAI Thu Jul 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1160493 (NAI Fri Nov 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1092128 (NAI Fri May 03 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1005492 (NAI Thu Jan 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources