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FDA Inspection
•Mibo Medical Group•September 30, 2019

Mibo Medical Group – FDA Inspection, Sep 30, 2019

Record Details

This FDA Inspection record concerns Mibo Medical Group, with an inspection on September 30, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Mibo Medical Group
Inspection Date
September 30, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Roy Baby (Company Rep)
View Company Profile

ID · 4667cd87-3d59-4f2d-b1ee-cf1a4afea06e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1105940
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Mibo Medical Group

1
DateClassificationOfficeProject area
May 10, 2018OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Mibo Medical Group
  • FDA Inspection 1051389 - 2018-05-10

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