FDA Inspection
Koning CorporationKoning Corporation – FDA Inspection, Jul 21, 2025
Record Details
This FDA Inspection record concerns Koning Corporation, with an inspection on July 21, 2025, issued by the Atlanta District Office, covering medical devices & rad health.
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ID · 8b2e8654-c34e-484c-b9d3-03ad2f54abb3
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1276569
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
FDA Citations
2- 21 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
- 21 CFR 801.20(a)Label to bear a unique device identifier
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Other FDA inspections of Koning Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 10, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 8, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 19, 2014 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Koning Corporation
- FDA Inspection 961418 - 2016-02-10
- FDA Inspection 886820 - 2014-07-08
- FDA Inspection 882197 - 2014-05-19
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