# Koning Corporation – FDA Inspection, Jul 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/koning-corporation/8b2e8654-c34e-484c-b9d3-03ad2f54abb3
Source feed: FDA_Inspections

> FDA inspection 1276569 of Koning Corporation, July 21, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR parts 801 and 830. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276569
- Company Name: Koning Corporation
- Inspection Date: 2025-07-21
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Atlanta District Office
- Citation Count: 2

## Related Documents

- [FDA Inspection 961418 - 2016-02-10](https://www.keypedia.com/records/fda_inspections/koning-corporation/fefeef1b-d00e-4b98-94c2-d78e84e7ad67)
- FDA Inspection 886820 - 2014-07-08
- FDA Inspection 882197 - 2014-05-19

## Related Officers

- [Company Rep](https://www.keypedia.com/people/nikki-s-bryant/fe859d4f-23a6-4bc9-94c6-5b3c3fe8d99a)

Company: https://www.keypedia.com/companies/koning-corporation/b5b7451a-7cf7-4713-91ec-1987fdda610e

Office: https://www.keypedia.com/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7