FDA Inspection 1067404 — Ionisos SAS

Ionisos SAS — FEI 3003775072

The FDA completed an inspection of Ionisos SAS on Jun 20, 2018 in Chaumesnil. 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
Jun 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Chaumesnil (France)