FDA Inspection 1056205 — Diagnostica Stago

Diagnostica Stago — FEI 3002806856

The FDA completed an inspection of Diagnostica Stago on Apr 12, 2018 in Franconville. 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 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Franconville (France)