FDA Inspection
Mediana Co., Ltd.Mediana Co., Ltd. – FDA Inspection, Sep 6, 2018
Record Details
This FDA Inspection record concerns Mediana Co., Ltd., with an inspection on September 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c3ef7a32-8deb-4f0c-9b29-1f1a11f185d9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1069071
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Mediana Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 24, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 9, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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