Company
United StatesVivaQuant, Inc., Arden Hills, MN – FDA Inspections
Inspection records and compliance data for VivaQuant, Inc. in Arden Hills, Minnesota. 2 FDA inspections on record, 1 Form 483, last inspected June 29, 2026.
Company Profile
This profile covers VivaQuant, Inc. based in Arden Hills, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected August 25, 2021. Last inspected June 29, 2026.
Most cited issue areas
- Corrective action records not maintained1 inspection
- Design and development procedures not documented1 inspection
- Design changes - Lack of or Inadequate Procedures1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| June 29, 2026 | Not classified | Medical Devices & Rad Health · Project Evaluation: Devices | 1318340 |
| August 25, 2021 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1150454 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
VivaQuant, Inc.
FEI Number
3011937459
Address
1265 Grey Fox Rd, ste 400, Arden Hills, Minnesota 55112, United States
Country
United States
ID: 214f5534-0477-4dd3-8543-4c2431485941