FDA Inspection
Eizo CorporationEizo Corporation – FDA Inspection, May 17, 2012
Record Details
This FDA Inspection record concerns Eizo Corporation, with an inspection on May 17, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Eizo Corporation
- Inspection Date
- May 17, 2012
- Product Type
- Devices
View Company Profile
ID · eb3a2738-1db1-49fb-b6b8-3ecd313424ae
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 786439
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Eizo Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 3, 2017 | Not classified | Office of Inspections and Investigations | |
| April 23, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Eizo Corporation
- FDA Inspection 1044096 - 2017-08-03
- FDA Inspection 929470 - 2015-04-23
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