FDA Inspection 754391 — NovaLung Gmbh

NovaLung Gmbh — FEI 3004569487

The FDA completed an inspection of NovaLung Gmbh on November 17, 2011 in Oberstenfeld. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 17, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Oberstenfeld (Germany)