# Mighty Oak Medical – FDA Inspection, May 9, 2025

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

> FDA inspection 1270686 of Mighty Oak Medical, May 09, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Denver District Office
- Citation Count: 2

## Related Documents

- FDA Inspection 1001291 - 2017-01-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

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