FDA Inspection 826656 — Aerolung Corp

Aerolung Corp — FEI 3008492927

The FDA completed an inspection of Aerolung Corp on April 9, 2013 in Largo, FL. 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
April 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Largo, FL (United States)