FDA Inspection 1001291 — Mighty Oak Medical, Inc.

Mighty Oak Medical, Inc. — FEI 3011818499

The FDA completed an inspection of Mighty Oak Medical, Inc. on January 13, 2017 in Englewood, CO. 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 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Englewood, CO (United States)