# FDA Inspection 695802 - Cepheid - October 29, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/cepheid/aafb4ab3-8235-49ab-911c-9ee1b682a584
Source feed: FDA_Inspections

> FDA Inspection 695802 for Cepheid on October 29, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695802
- Company Name: Cepheid
- Inspection Date: 2010-10-29
- Classification: Voluntary Action Indicated (VAI)
- 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