FDA Inspection 1019828 — Medacta International SA

Medacta International SA — FEI 3008110533

The FDA completed an inspection of Medacta International SA on June 19, 2017 in Castel San Pietro. 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
June 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Castel San Pietro (Switzerland)