FDA Inspection 909484 — Kulzer Gmbh

Kulzer Gmbh — FEI 3002807166

The FDA completed an inspection of Kulzer Gmbh on December 11, 2014 in Wehrheim. 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 11, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Wehrheim (Germany)