# FDA Inspection 961418 - Koning Corporation - February 10, 2016

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

> FDA Inspection 961418 for Koning Corporation on February 10, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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