# FDA Inspection 1070529 - R82 A/S - November 01, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/r82-as/23fbd5e9-7fc0-4725-b5ec-444eb149cd9d
Source feed: FDA_Inspections

> FDA Inspection 1070529 for R82 A/S on November 01, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070529
- Company Name: R82 A/S
- Inspection Date: 2018-11-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1070529 - 2018-11-01](https://www.globalkeysolutions.net/records/fda_inspections/r82-as/f25bf9f4-63b7-4a3e-ab0e-8a1332b8bd5d)
- [FDA Inspection 839344 - 2013-06-07](https://www.globalkeysolutions.net/records/fda_inspections/r82-as/c8f263dd-b665-4c8c-bceb-577d6e7f0a13)
- [FDA Inspection 697737 - 2010-10-07](https://www.globalkeysolutions.net/records/fda_inspections/r82-as/18419a31-888f-4445-9009-79684a21f970)

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