# FDA Inspection 600366 - Autogenesis Inc - July 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/autogenesis-inc/e953856f-17cc-465d-8897-e11101459df0
Source feed: FDA_Inspections

> FDA Inspection 600366 for Autogenesis Inc on July 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 600366
- Company Name: Autogenesis Inc
- Inspection Date: 2009-07-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 861124 - 2013-12-17](https://www.keypedia.com/records/fda_inspections/autogenesis-inc/3e2a1c67-d6ab-4448-96cf-926b25c0e004)
- [FDA Inspection 861124 - 2013-12-17](https://www.keypedia.com/records/fda_inspections/autogenesis-inc/f5c65349-5198-498c-9cb0-95eacf2950c7)

Company: https://www.keypedia.com/companies/autogenesis-inc/de870aeb-561d-41aa-b46e-660941c67d1f

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