# Genesis Northwest, Incorporated – FDA Inspection, Aug 5, 2009

Source: https://www.keypedia.com/records/fda_inspections/genesis-northwest-incorporated/65ec8d92-50c6-40d4-951c-446d88289ae5
Source feed: FDA_Inspections

> FDA inspection 601998 of Genesis Northwest, Incorporated, August 05, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 601998
- Company Name: Genesis Northwest, Incorporated
- Inspection Date: 2009-08-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 914219 - 2015-02-13
- FDA Inspection 813365 - 2013-01-18
- FDA Inspection 701973 - 2010-11-30

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