# FDA Inspection 733296 - GN Resound North America - June 28, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/gn-resound-north-america/12c4348a-670c-4124-ac83-facb2cd43f39
Source feed: FDA_Inspections

> FDA Inspection 733296 for GN Resound North America on June 28, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 733296
- Company Name: GN Resound North America
- Inspection Date: 2011-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7