FDA Inspection 799433 — Z-SYSTEMS AG

Z-SYSTEMS AG — FEI 3006948427

The FDA completed an inspection of Z-SYSTEMS AG on Sep 13, 2012 in Oensingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

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

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