# FDA Inspection 878349 - DFINE Inc. - May 12, 2014

Source: https://www.keypedia.com/records/fda_inspections/dfine-inc/11b5aee0-9d5b-4a16-8f1d-b45214fc9736
Source feed: FDA_Inspections

> FDA Inspection 878349 for DFINE Inc. on May 12, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 878349
- Company Name: DFINE Inc.
- Inspection Date: 2014-05-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 878349 - 2014-05-12](https://www.keypedia.com/records/fda_inspections/dfine-inc/d6fa992d-6de9-46fa-b1af-c57f1c732c77)
- [FDA Inspection 571157 - 2009-03-13](https://www.keypedia.com/records/fda_inspections/dfine-inc/039db44a-336b-4af7-8217-840f42e0417e)
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Company: https://www.keypedia.com/companies/dfine-inc/431f4e9c-5a00-43a4-9383-a7c3c7475d40

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