FDA Inspection 860797 — Sutter Medizintechnik GmbH

Sutter Medizintechnik GmbH — FEI 3004857377

The FDA completed an inspection of Sutter Medizintechnik GmbH on December 12, 2013 in Emmendingen. 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
December 12, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Emmendingen (Germany)