# Koven Technology, Inc. – FDA Inspection, Nov 15, 2022

Source: https://www.keypedia.com/records/fda_inspections/koven-technology-inc/2b442da0-f3cb-4791-a590-2a0d54f0afff
Source feed: FDA_Inspections

> FDA inspection 1191634 of Koven Technology, Inc., November 15, 2022. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1191634
- Company Name: Koven Technology, Inc.
- Inspection Date: 2022-11-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1301788 - 2026-02-06](https://www.keypedia.com/records/fda_inspections/koven-technology-inc/76f0a970-b3dd-45ce-9308-9fc17ee38007)
- [FDA Inspection 1030726 - 2017-11-03](https://www.keypedia.com/records/fda_inspections/koven-technology-inc/374f17e6-26a1-43c6-846b-07651b56f007)

Company: https://www.keypedia.com/companies/koven-technology-inc/2a1f4139-f4b1-4a2f-9b20-53bdec21f5e4

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