FDA Inspection 1007067 — Technix S.P.A

Technix S.P.A — FEI 3008044777

The FDA completed an inspection of Technix S.P.A on Feb 3, 2017 in Grassobbio. 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
Feb 3, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Grassobbio (Italy)

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