# Koven Technology, Inc., Saint Louis, MO – FDA Inspections

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

> Inspection records and compliance data for Koven Technology, Inc. in Saint Louis, Missouri. 3 FDA inspections on record, 2 Form 483s, last inspected February 06, 2026.

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## Details

- Name: Koven Technology, Inc.
- FEI Number: 1937397
- Address Line 1: 477 N Lindbergh Blvd Ste 220
- City: Saint Louis
- State: Missouri
- Zip Code: 63141
- Country Name: United States
- Address: 477 N Lindbergh Blvd Ste 220, Saint Louis, Missouri 63141, United States
- Country: United States

## Related Documents

- [483 - Koven Technology, Inc. - 2026-02-06](https://www.keypedia.com/records/483/koven-technology-inc/f6f56e86-90f3-42ff-be09-0ca848d0038d) — source: FDA, date: February 6, 2026
- FDA Inspection 1301788 - Koven Technology, Inc. - 2026-02-06 — source: FDA, date: February 6, 2026
- [FDA Inspection 1301788 - Koven Technology, Inc. - 2026-02-06](https://www.keypedia.com/records/fda_inspections/koven-technology-inc/76f0a970-b3dd-45ce-9308-9fc17ee38007) — source: FDA, date: February 6, 2026
- [FDA Inspection 1191634 - Koven Technology, Inc. - 2022-11-15](https://www.keypedia.com/records/fda_inspections/koven-technology-inc/2b442da0-f3cb-4791-a590-2a0d54f0afff) — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2022
- FDA Inspection 1191634 - Koven Technology, Inc. - 2022-11-15 — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2022
- [FDA Inspection 1030726 - Koven Technology, Inc. - 2017-11-03](https://www.keypedia.com/records/fda_inspections/koven-technology-inc/374f17e6-26a1-43c6-846b-07651b56f007) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2017
- FDA Inspection 1030726 - Koven Technology, Inc. - 2017-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2017

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