# GN Resound North America - Inspection Records

Source: https://www.globalkeysolutions.net/companies/gn-resound-north-america/0903ad7b-8e55-4b75-b741-9574a7d1824a

> Inspection records and compliance data for GN Resound North America in Bloomington, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: GN Resound North America
- FEI Number: 2182204
- City: Bloomington
- State: Minnesota
- Country Name: United States
- Address Line 1: 8001 E Bloomington Fwy
- Zip Code: 55420

## Related Documents

- [FDA Inspection 1037254 - GN Resound North America - 2018-01-10](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/5518cab9-099d-4c60-8677-46ad8fe0ceda) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2018
- [FDA Inspection 824925 - GN Resound North America - 2013-04-01](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/5ccfbdcf-5e2f-4655-9bd3-358661085327) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- [FDA Inspection 824925 - GN Resound North America - 2013-04-01](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/03397ab9-5bc6-46f2-94db-d6792babd861) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- [FDA Inspection 733296 - GN Resound North America - 2011-06-28](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/12c4348a-670c-4124-ac83-facb2cd43f39) — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2011
- [FDA Inspection 662331 - GN Resound North America - 2010-05-17](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/8c82206c-f7ee-40bf-9a4c-eb9f09b5412b) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2010
- [FDA Inspection 661850 - GN Resound North America - 2010-04-28](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/0367fd57-a82a-4f5c-885b-5fee429a09a2) — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2010
- [FDA Inspection 661850 - GN Resound North America - 2010-04-28](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/a8f00d95-7ade-46b3-a63c-5cbb171e8da1) — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2010
- [FDA Inspection 579054 - GN Resound North America - 2009-04-22](https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/0fd64159-2073-4c72-9288-61b91f975167) — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2009

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