# FDA Inspection 559037 - R82 Incorporated - January 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/r82-incorporated/aec60e57-44a1-4f51-a83b-bff055ab7978
Source feed: FDA_Inspections

> FDA Inspection 559037 for R82 Incorporated on January 16, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559037
- Company Name: R82 Incorporated
- Inspection Date: 2009-01-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988829 - 2016-09-21](https://www.keypedia.com/records/fda_inspections/r82-incorporated/0e32f337-1347-48f3-9b21-92234dc9d693)
- [FDA Inspection 559037 - 2009-01-16](https://www.keypedia.com/records/fda_inspections/r82-incorporated/90933429-0053-4296-a5bd-10b36776801d)

Company: https://www.keypedia.com/companies/r82-incorporated/2f552a8c-41e9-43ed-8ffd-934a53bbcfee

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