# FDA Inspection 820660 - Fujirebio Diagnostics, Inc. - February 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/fujirebio-diagnostics-inc/500499b3-b098-4e80-8d77-6cb6b6522a11
Source feed: FDA_Inspections

> FDA Inspection 820660 for Fujirebio Diagnostics, Inc. on February 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820660
- Company Name: Fujirebio Diagnostics, Inc.
- Inspection Date: 2013-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 820660 - 2013-02-15](https://www.keypedia.com/records/fda_inspections/fujirebio-diagnostics-inc/31f6ac01-6a1c-4120-8542-5e553486b263)
- [FDA Inspection 730805 - 2011-06-17](https://www.keypedia.com/records/fda_inspections/fujirebio-diagnostics-inc/d35ce233-30d7-4ebc-8110-2a5ec953cb2b)

Company: https://www.keypedia.com/companies/fujirebio-diagnostics-inc/db1006a5-f440-4d72-b586-550e0985a4a1

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