FDA Inspection 822370 — NovaLung Gmbh

NovaLung Gmbh — FEI 3004569487

The FDA completed an inspection of NovaLung Gmbh on March 14, 2013 in Oberstenfeld. 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 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Oberstenfeld (Germany)