FDA Inspection
Mighty Oak MedicalMighty Oak Medical – FDA Inspection, May 9, 2025
Record Details
This FDA Inspection record concerns Mighty Oak Medical, with an inspection on May 9, 2025, issued by the Denver District Office, covering medical devices & rad health.
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ID · e46b6270-4320-42d0-bf4a-3f1988f514d2
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1270686
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
FDA Citations
2- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Mighty Oak Medical
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mighty Oak Medical
- FDA Inspection 1001291 - 2017-01-13
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