FDA Inspection 1020927 — Artsana S.p.A.

Artsana S.p.A. — FEI 3002807528

The FDA completed an inspection of Artsana S.p.A. on July 20, 2017 in Casnate Con Bernate. 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
July 20, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Casnate Con Bernate (Italy)