FDA Inspection 567235 — INNOVIEW GMBH

INNOVIEW GMBH — FEI 3003922255

The FDA completed an inspection of INNOVIEW GMBH on January 28, 2009 in Eichstetten. 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
January 28, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Eichstetten (Germany)