# FDA Inspection 973307 - Fujirebio Inc - May 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujirebio-inc/cc042f75-2e08-4581-b268-3f888477e83b
Source feed: FDA_Inspections

> FDA Inspection 973307 for Fujirebio Inc on May 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 973307
- Company Name: Fujirebio Inc
- Inspection Date: 2016-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 973307 - 2016-05-19](https://www.globalkeysolutions.net/records/fda_inspections/fujirebio-inc/0ac4e912-1a59-47b2-abd0-18a83560421f)
- [FDA Inspection 973307 - 2016-05-19](https://www.globalkeysolutions.net/records/fda_inspections/fujirebio-inc/dbccb22f-0f8e-4b7f-84ce-19efa4f755f7)

Company: https://www.globalkeysolutions.net/companies/fujirebio-inc/a7eb6a44-3f78-4c1b-8a7d-9a073ff9548c

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