# Koning Corporation – FDA Inspection, Feb 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/koning-corporation/fefeef1b-d00e-4b98-94c2-d78e84e7ad67
Source feed: FDA_Inspections

> FDA inspection 961418 of Koning Corporation, February 10, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961418
- Company Name: Koning Corporation
- Inspection Date: 2016-02-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1276569 - 2025-07-21](https://www.keypedia.com/records/fda_inspections/koning-corporation/8b2e8654-c34e-484c-b9d3-03ad2f54abb3)
- FDA Inspection 886820 - 2014-07-08
- FDA Inspection 882197 - 2014-05-19

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7