FDA Inspection 718125 — Aerogen Ltd.

Aerogen Ltd. — FEI 3004127293

The FDA completed an inspection of Aerogen Ltd. on March 31, 2011 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
March 31, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)