FDA Inspection
Kaneka CorporationKaneka Corporation – FDA Inspection, Apr 19, 2017
Record Details
This FDA Inspection record concerns Kaneka Corporation, with an inspection on April 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · db652a43-7e4f-4a25-9a8c-13d9bfa40c1a
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1012619
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Kaneka Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2025 | VAI | Office of Inspections and Investigations | Compliance: Medical Devices |
| March 3, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 13, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kaneka Corporation
- FDA Inspection 1260082 - 2025-02-06
- FDA Inspection 962212 - 2016-03-03
- FDA Inspection 800241 - 2012-09-13
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