FDA Inspection 1055692 — Diagnostica Stago

Diagnostica Stago — FEI 3001573851

The FDA completed an inspection of Diagnostica Stago on Apr 10, 2018 in Gennevilliers. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 10, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Gennevilliers (France)