# FDA Inspection 1026773 - Cepheid - August 09, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/cepheid/2547e939-ff56-41fe-8434-fe7d3e52c57f
Source feed: FDA_Inspections

> FDA Inspection 1026773 for Cepheid on August 09, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026773
- Company Name: Cepheid
- Inspection Date: 2017-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/cepheid/b8ab5e76-7447-435e-a3e3-c387ac1c40ec

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