# FDA Inspection 914219 - Genesis Northwest, Incorporated - February 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/genesis-northwest-incorporated/b8df2700-55d8-415f-b096-42942eb31009
Source feed: FDA_Inspections

> FDA Inspection 914219 for Genesis Northwest, Incorporated on February 13, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 914219
- Company Name: Genesis Northwest, Incorporated
- Inspection Date: 2015-02-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 813365 - 2013-01-18](https://www.keypedia.com/records/fda_inspections/genesis-northwest-incorporated/f5363853-42e3-46a9-93d6-587b0ccb1e8c)
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Company: https://www.keypedia.com/companies/genesis-northwest-incorporated/ec1cce59-34b3-401f-9a3e-b2fc80399672

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