FDA Inspection 754525 — Vyaire Medical

Vyaire Medical — FEI 3002617992

The FDA completed an inspection of Vyaire Medical on November 25, 2011 in Minneapolis, MN. 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
November 25, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)