# FDA Inspection 697737 - R82 A/S - October 07, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/r82-as/18419a31-888f-4445-9009-79684a21f970
Source feed: FDA_Inspections

> FDA Inspection 697737 for R82 A/S on October 07, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 697737
- Company Name: R82 A/S
- Inspection Date: 2010-10-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/r82-as/e9d511e0-668f-4cf2-ae91-f6a4de786d70

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