FDA Inspection 1070002 — Tecnimed S.R.L.

Tecnimed S.R.L. — FEI 3003334361

The FDA completed an inspection of Tecnimed S.R.L. on Sep 5, 2018 in Vedano Olona. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 5, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Vedano Olona (Italy)