# Access Point Technologies - Inspection Records

Source: https://www.globalkeysolutions.net/companies/access-point-technologies/a59bb412-c7cb-4825-b925-eed9ed738136

> Inspection records and compliance data for Access Point Technologies in Rogers, Minnesota. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [483 - Access Point Technologies - 2022-12-20](https://www.globalkeysolutions.net/records/483/access-point-technologies/6be2a62a-15ca-495f-9f00-b8703b9c5057) — source: FDA, date: December 20, 2022
- [FDA Inspection 1194801 - Access Point Technologies - 2022-12-20](https://www.globalkeysolutions.net/records/fda_inspections/access-point-technologies/f5fb0203-0024-4e58-b1c3-03385196213a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2022
- [FDA Inspection 1194801 - Access Point Technologies - 2022-12-20](https://www.globalkeysolutions.net/records/fda_inspections/access-point-technologies/6a896c7c-1af6-4949-8438-d56c4f87f908) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2022
- [FDA Inspection 1001757 - Access Point Technologies - 2017-02-23](https://www.globalkeysolutions.net/records/fda_inspections/access-point-technologies/92c6d9bb-c86d-40ea-807c-7f31ac6c72f4) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2017
- [FDA Inspection 845090 - Access Point Technologies - 2013-07-16](https://www.globalkeysolutions.net/records/fda_inspections/access-point-technologies/4410d403-9e47-4ef3-9d54-2ca6e3797e3a) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2013
- [FDA Inspection 648455 - Access Point Technologies - 2010-03-04](https://www.globalkeysolutions.net/records/fda_inspections/access-point-technologies/5327ffd9-0d20-4e5e-a119-cde81b980301) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2010

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