Facility

ACCESS POINT TECHNOLOGIES, EP INC.

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)	3005402529
Establishment type	Manufacture Device in the United States for Export Only
Location	12560 FLETCHER LANE Rogers, MN, US 55374
Registration status	Active · expires 2026
Parent company	Stereotaxis (owner-operator 9048165)
Brand names	Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
Product code OAE (opens in a new tab) · Class III · Unknown

Recalls & enforcement

Class IITerminated2020-09-21
There is a potential for fire in the inside computer cabinet.

FDA inspections (3)

VAI2026-05-01
Voluntary Action Indicated · Compliance: Devices · citations posted
NAI2022-12-20
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2017-02-23
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.

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. “ACCESS POINT TECHNOLOGIES, EP INC. (FEI 3005402529) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005402529-access-point-technologies-ep-inc/

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