# FDA Inspection 561498 - Fujifilm Irvine Scientific, Inc. - January 20, 2009

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-irvine-scientific-inc/b8cd9f0e-02e7-4b31-a723-5c1f9d9bff38
Source feed: FDA_Inspections

> FDA Inspection 561498 for Fujifilm Irvine Scientific, Inc. on January 20, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 561498
- Company Name: Fujifilm Irvine Scientific, Inc.
- Inspection Date: 2009-01-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 886130 - 2014-07-02](https://www.keypedia.com/records/fda_inspections/fujifilm-irvine-scientific-inc/d6fe786c-7cd2-4b2d-83b1-a1f25f39d07e)
- [FDA Inspection 886130 - 2014-07-02](https://www.keypedia.com/records/fda_inspections/fujifilm-irvine-scientific-inc/bd86aecc-d9af-4919-bdee-a24e6931f50b)
- [FDA Inspection 561498 - 2009-01-20](https://www.keypedia.com/records/fda_inspections/fujifilm-irvine-scientific-inc/4cd73109-75ee-4ce3-9abf-714e99a06c5a)

Company: https://www.keypedia.com/companies/fujifilm-irvine-scientific-inc/a629768f-913e-463a-99fd-11630b18e967

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