FDA Inspection 815800 — GVS SpA

GVS SpA — FEI 3003624034

The FDA completed an inspection of GVS SpA on Oct 18, 2012 in Zola Predosa. 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
Oct 18, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Zola Predosa (Italy)

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