FEI 3008513054
Koning Corporation
5555 Oakbrook Pkwy Ste 640, Norcross, GA, US
MDR events0All time
Recalls0All time
Registered products1
Establishment typeComplaintComplaint File Establishment per 21 CFR 820.198
Registered product codes
1 product codes
Recent MDR events
0 on file
No MDR events on file for this firm name.
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3008513054.
FDA inspections
3 on file
- Voluntary Action Indicated (VAI)Jul 21, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Jul 21, 2025
Postmarket Assurance: Devices · Citations posted
- No Action Indicated (NAI)Jul 21, 2025
Radiation Control and Health Safety Act · Citations posted
Inspection citations
2 on file
Top cited requirements
Compare to industry ↗- 21 CFR 801.20(a)Jul 21, 2025
Label to bear a unique device identifier
- 21 CFR 830.300(a)Jul 21, 2025
Devices subject to device identification GUDID data submission requirements.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.