FDA Inspection 762578 — Vyaire Medical

Vyaire Medical — FEI 3013421741

The FDA completed an inspection of Vyaire Medical on Jan 10, 2012 in Mettawa, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Mettawa, IL (United States)