# FDA Inspection 1301590 - Michael Moront MD - January 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/michael-moront-md/95cd05d1-3380-4d2a-acc3-f4cbc29620a9
Source feed: FDA_Inspections

> FDA Inspection 1301590 for Michael Moront MD on January 12, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1301590
- Company Name: Michael Moront MD
- Inspection Date: 2026-01-12
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices

## Related Documents

- [FDA Inspection 1301590 - 2026-01-12](https://www.keypedia.com/records/fda_inspections/michael-moront-md/6e2c8501-fe21-4de4-ad43-d5e791988666)
- [FDA Inspection 1013073 - 2017-05-26](https://www.keypedia.com/records/fda_inspections/michael-moront-md/28b33092-76e2-4a4e-8388-163d3fc29396)

Company: https://www.keypedia.com/companies/michael-moront-md/fe2d445c-9458-4fb0-903b-23805a4e18ee