# Mibo Medical Group – FDA Inspection, May 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/mibo-medical-group/d13d5cc9-dfef-4f80-880e-6711c445915e
Source feed: FDA_Inspections

> FDA inspection 1051389 of Mibo Medical Group, May 10, 2018. Classification: Official Action Indicated (OAI). 9 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051389
- Company Name: Mibo Medical Group
- Inspection Date: 2018-05-10
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- [FDA Inspection 1105940 - 2019-09-30](https://www.keypedia.com/records/fda_inspections/mibo-medical-group/4667cd87-3d59-4f2d-b1ee-cf1a4afea06e)

## 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