# FDA Inspection 1030726 - Koven Technology, Inc. - November 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/koven-technology-inc/374f17e6-26a1-43c6-846b-07651b56f007
Source feed: FDA_Inspections

> FDA Inspection 1030726 for Koven Technology, Inc. on November 03, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030726
- Company Name: Koven Technology, Inc.
- Inspection Date: 2017-11-03
- 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.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