# Access Point Technologies EP, Inc., Rogers, MN – FDA Inspections

Source: https://www.keypedia.com/companies/access-point-technologies-ep-inc/a59bb412-c7cb-4825-b925-eed9ed738136

> Inspection records and compliance data for Access Point Technologies EP, Inc. in Rogers, Minnesota. 5 FDA inspections on record, 1 Form 483, last inspected May 01, 2026.

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## Details

- Name: Access Point Technologies EP, Inc.
- FEI Number: 3005402529
- Address Line 1: 12560 Fletcher Ln Ste 300
- City: Rogers
- State: Minnesota
- Zip Code: 55374
- Country Name: United States
- Address: 12560 Fletcher Ln Ste 300, Rogers, Minnesota 55374, United States
- Country: United States

## Related Documents

- [FDA Inspection 1315018 - Access Point Technologies EP, Inc. - 2026-05-01](https://www.keypedia.com/records/fda_inspections/access-point-technologies-ep-inc/54757991-1545-45fb-a1a6-26716136211d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2026
- [483 - Access Point Technologies EP, Inc. - 2022-12-20](https://www.keypedia.com/records/483/access-point-technologies-ep-inc/6be2a62a-15ca-495f-9f00-b8703b9c5057) — source: FDA, date: December 20, 2022
- FDA Inspection 1194801 - Access Point Technologies EP, Inc. - 2022-12-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2022
- FDA Inspection 1194801 - Access Point Technologies EP, Inc. - 2022-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2022
- FDA Inspection 1001757 - Access Point Technologies EP, Inc. - 2017-02-23 — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2017
- FDA Inspection 845090 - Access Point Technologies EP, Inc. - 2013-07-16 — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2013
- [FDA Inspection 648455 - Access Point Technologies EP, Inc. - 2010-03-04](https://www.keypedia.com/records/fda_inspections/access-point-technologies-ep-inc/5327ffd9-0d20-4e5e-a119-cde81b980301) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2010

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