FDA Inspection 799433 — Z-SYSTEMS AG

Z-SYSTEMS AG — FEI 3006948427

The FDA completed an inspection of Z-SYSTEMS AG on September 13, 2012 in Oensingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Oensingen (Switzerland)