# FDA Inspection 1023448 - Diagnostics Direct LLC - August 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/diagnostics-direct-llc/c42abf6c-63db-4842-9b60-76a664ae834a
Source feed: FDA_Inspections

> FDA Inspection 1023448 for Diagnostics Direct LLC on August 30, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023448
- Company Name: Diagnostics Direct LLC
- Inspection Date: 2017-08-30
- 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 1023448 - 2017-08-30](https://www.keypedia.com/records/fda_inspections/diagnostics-direct-llc/804bab10-4b95-418c-82d8-daa66ac096ec)
- [FDA Inspection 851750 - 2013-07-03](https://www.keypedia.com/records/fda_inspections/diagnostics-direct-llc/7bfb50a5-868d-43f1-9e20-0493441107ec)
- [FDA Inspection 851750 - 2013-07-03](https://www.keypedia.com/records/fda_inspections/diagnostics-direct-llc/82c8d8d0-be05-429e-8fd0-70345e3691d9)

Company: https://www.keypedia.com/companies/diagnostics-direct-llc/18bb832c-8d5d-4ff0-b22e-65bb6348ca13

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