Company
United StatesVirtex, Anoka, MN – FDA Inspections
Inspection records and compliance data for Virtex in Anoka, Minnesota. 2 FDA inspections on record, last inspected April 19, 2024.
Company Profile
This profile covers Virtex based in Anoka, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Form 483s
- 0
- Warning letters
- 0
First inspected September 12, 2019. Last inspected April 19, 2024.
Most cited issue areas
- Production and Process Change Procedures, lack of or Inad.1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| April 19, 2024 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1236405 |
| September 12, 2019 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1102921 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Virtex
FEI Number
2183673
Address
6700 Bunker Lake Blvd Nw, Anoka, Minnesota 55303, United States
Country
United States
ID: 6467c19e-8ab1-4038-a523-b5ba040310e6