# FDA Inspection 1270686 - Mighty Oak Medical - May 09, 2025

Source: https://www.keypedia.com/records/fda_inspections/mighty-oak-medical/e46b6270-4320-42d0-bf4a-3f1988f514d2
Source feed: FDA_Inspections

> FDA Inspection 1270686 for Mighty Oak Medical on May 09, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1270686
- Company Name: Mighty Oak Medical
- Inspection Date: 2025-05-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Denver District Office

## Related Documents

- [FDA Inspection 1270686 - 2025-05-09](https://www.keypedia.com/records/fda_inspections/mighty-oak-medical/9a6d42e1-1174-4e13-8bfc-390cdf74dd4f)
- [FDA Inspection 1270686 - 2025-05-09](https://www.keypedia.com/records/fda_inspections/mighty-oak-medical/4abd844c-9966-4120-b9a9-8e0cf285e879)
- [FDA Inspection 1270686 - 2025-05-09](https://www.keypedia.com/records/fda_inspections/mighty-oak-medical/fbf4b452-8fe2-4602-847a-8c04dbf13be5)
- [FDA Inspection 1001291 - 2017-01-13](https://www.keypedia.com/records/fda_inspections/mighty-oak-medical/fb4359b5-2091-4728-9a92-6e6ea1fa7076)

Company: https://www.keypedia.com/companies/mighty-oak-medical/89c8a0f3-2b3a-4f33-bfe1-34f5c9eea05b

Office: https://www.keypedia.com/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face