FDA Inspection 892023 — Ziehm Imaging Gmbh

Ziehm Imaging Gmbh — FEI 3005430103

The FDA completed an inspection of Ziehm Imaging Gmbh on Aug 7, 2014 in Nuremberg. 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
Aug 7, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Nuremberg (Germany)

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