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FDA Inspection 1090414 — Lumibird Medical Inc

Lumibird Medical Inc — FEI 1000520094

The FDA completed an inspection of Lumibird Medical Inc on May 7, 2019 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
May 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Eden Prairie, MN (United States)

Facility

Other inspections at this facility

  • 1004044 (NAI Wed Jan 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 962771 (NAI Wed Mar 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources