# FDA Inspection 1105940 - Mibo Medical Group - September 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/mibo-medical-group/4667cd87-3d59-4f2d-b1ee-cf1a4afea06e
Source feed: FDA_Inspections

> FDA Inspection 1105940 for Mibo Medical Group on September 30, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1105940
- Company Name: Mibo Medical Group
- Inspection Date: 2019-09-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1105940 - 2019-09-30](https://www.keypedia.com/records/fda_inspections/mibo-medical-group/43b299cb-6b14-486a-9ab1-70128632f273)
- [FDA Inspection 1051389 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/mibo-medical-group/2da92b1f-7191-40df-8d66-7e71ef7346b2)
- [FDA Inspection 1051389 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/mibo-medical-group/d13d5cc9-dfef-4f80-880e-6711c445915e)

Company: https://www.keypedia.com/companies/mibo-medical-group/1259e745-1838-466d-b0ea-df534190b522

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