# FDA Inspection 1001172 - DFB Technologies, Ltd - January 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/dfb-technologies-ltd/101fc3a7-0631-4238-9e05-35f799fb5ff3
Source feed: FDA_Inspections

> FDA Inspection 1001172 for DFB Technologies, Ltd on January 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001172
- Company Name: DFB Technologies, Ltd
- Inspection Date: 2017-01-19
- 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 1001172 - 2017-01-19](https://www.keypedia.com/records/fda_inspections/dfb-technologies-ltd/05718581-b4b3-438d-8a01-ffb0e1e4ced4)
- [FDA Inspection 738840 - 2011-08-09](https://www.keypedia.com/records/fda_inspections/dfb-technologies-ltd/f825fea1-ff03-4371-994c-cbfab6a12a5f)
- [FDA Inspection 738840 - 2011-08-09](https://www.keypedia.com/records/fda_inspections/dfb-technologies-ltd/36986c57-196d-436f-832f-2e4aefd85a96)

Company: https://www.keypedia.com/companies/dfb-technologies-ltd/cf2a5c97-a5a4-42c8-9834-42940a1461de

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