FDA Inspection 991562 — Vyaire Medical Oy

Vyaire Medical Oy — FEI 3010838917

The FDA completed an inspection of Vyaire Medical Oy on September 29, 2016 in Helsinki. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Helsinki (Finland)