FDA Inspection 941408 — Somatex Medical Technologies GMBH

Somatex Medical Technologies GMBH — FEI 1000408433

The FDA completed an inspection of Somatex Medical Technologies GMBH on September 10, 2015 in Berlin. 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
September 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Berlin (Germany)