FDA Inspection 1070447 — Barco N.V.

Barco N.V. — FEI 3004455125

The FDA completed an inspection of Barco N.V. on September 21, 2018 in Kortrijk. 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
September 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kortrijk (Belgium)