FDA Inspection 1062145 — Aerogen Ltd.

Aerogen Ltd. — FEI 3004127293

The FDA completed an inspection of Aerogen Ltd. on May 11, 2018 in Galway. 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
May 11, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)