Company
United StatesKoven Technology, Inc., Saint Louis, MO – FDA Inspections
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.
Company Profile
This profile covers Koven Technology, Inc. based in Saint Louis, Missouri, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 2
- Warning letters
- 0
First inspected November 3, 2017. Last inspected February 6, 2026.
Most cited issue areas
- Criteria for the evaluation and selection of suppliers not established1 inspection
- Design changes - Lack of or Inadequate Procedures1 inspection
- Records for complaints involving failure to meet specifications not maintained1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| February 6, 2026 | Not classified | Medical Devices & Rad Health · Compliance: Medical Devices | 1301788 |
| November 15, 2022 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1191634 |
| November 3, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1030726 |
FDA documents
Form 483s (1)
People (1)
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Koven Technology, Inc.
FEI Number
1937397
Address
477 N Lindbergh Blvd Ste 220, Saint Louis, Missouri 63141, United States
Country
United States
ID: 2a1f4139-f4b1-4a2f-9b20-53bdec21f5e4