FDA Inspection 1004044 — Lumibird Medical Inc

Lumibird Medical Inc — FEI 1000520094

The FDA completed an inspection of Lumibird Medical Inc on January 18, 2017 in Eden Prairie, 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
January 18, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)