FDA Inspection 1110194 — Ionisos

Ionisos — FEI 3003110073

The FDA completed an inspection of Ionisos on October 24, 2019 in Dagneux. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 24, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Dagneux (France)