FDA Inspection 1270686 — Mighty Oak Medical, Inc.

Mighty Oak Medical, Inc. — FEI 3011818499

The FDA completed an inspection of Mighty Oak Medical, Inc. on May 9, 2025 in Englewood, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 9, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Englewood, CO (United States)

Citations

IDCFRDescription
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures