FDA Inspection
Koven Technology, Inc.Koven Technology, Inc. – FDA Inspection, Nov 3, 2017
Record Details
This FDA Inspection record concerns Koven Technology, Inc., with an inspection on November 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 374f17e6-26a1-43c6-846b-07651b56f007
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030726
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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Other FDA inspections of Koven Technology, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | Not classified | Kansas City District Office | Compliance: Medical Devices |
| November 15, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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