# FDA Inspection 1276569 - Koning Corporation - July 21, 2025

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

> FDA Inspection 1276569 for Koning Corporation on July 21, 2025. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Atlanta District Office

## Related Documents

- [FDA Inspection 1276569 - 2025-07-21](https://www.globalkeysolutions.net/api/records/fda_inspections/koning-corporation/48b76be4-4c9d-4579-9e5d-c1fa1272999a/)
- [FDA Inspection 1276569 - 2025-07-21](https://www.globalkeysolutions.net/api/records/fda_inspections/koning-corporation/f2f17a93-2b16-4adb-8209-590473be3724/)
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- [FDA Inspection 1276569 - 2025-07-21](https://www.globalkeysolutions.net/api/records/fda_inspections/koning-corporation/d4803a91-5ceb-459c-967f-67fcfe4d5724/)

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

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