# FDA Inspection 1013073 - Michael Moront MD - May 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/michael-moront-md/28b33092-76e2-4a4e-8388-163d3fc29396
Source feed: FDA_Inspections

> FDA Inspection 1013073 for Michael Moront MD on May 26, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1013073
- Company Name: Michael Moront MD
- Inspection Date: 2017-05-26
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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 1301590 - 2026-01-12](https://www.keypedia.com/records/fda_inspections/michael-moront-md/95cd05d1-3380-4d2a-acc3-f4cbc29620a9)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7