# Mibo Medical Group – FDA Inspection, Sep 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 of Mibo Medical Group, September 30, 2019. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1105940
- Company Name: Mibo Medical Group
- Inspection Date: 2019-09-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1051389 - 2018-05-10](https://www.keypedia.com/records/fda_inspections/mibo-medical-group/d13d5cc9-dfef-4f80-880e-6711c445915e)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

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