FDA Inspection 909484 — Kulzer Gmbh

Kulzer Gmbh — FEI 3002807166

The FDA completed an inspection of Kulzer Gmbh on Dec 11, 2014 in Wehrheim. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 11, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Wehrheim (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.