Facility

VIRTUAL RADIOLOGIC CORPORATION

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

3inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3007795813
Establishment type	Manufacture Medical Device
Location	3600 Minnesota Dr Ste 800 Edina, MN, US 55435
Registration status	Active · expires 2026
Parent company	Virtual Radiologic Corporation (owner-operator 10029207)
Brand names	vRad Viewer; Mosaic Viewer

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

System, Image Processing, Radiological
Product code LLZ (opens in a new tab) · Class II · Radiology · 21 CFR 892.2050

Recalls & enforcement

Class IIOngoing2023-05-09
The error resulted in intermittent failure of current (primary) radiology study images not displaying to the interpreting teleradiologist.

FDA inspections (3)

VAI2026-03-05
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2022-05-26
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2016-12-09
No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by Virtual Radiologic Corporation

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “VIRTUAL RADIOLOGIC CORPORATION (FEI 3007795813) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007795813-virtual-radiologic-corporation/

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