# Cepheid – FDA Inspection, Jun 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/cepheid/da35e071-bda6-4198-8e8a-7f2abbcf740c
Source feed: FDA_Inspections

> FDA inspection 928802 of Cepheid, June 16, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 928802
- Company Name: Cepheid
- Inspection Date: 2015-06-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1026773 - 2017-08-09
- FDA Inspection 763635 - 2012-01-13
- [FDA Inspection 695802 - 2010-10-29](https://www.keypedia.com/records/fda_inspections/cepheid/c7096018-7f22-4e9e-837c-29fca4c4b4e1)
- FDA Inspection 612704 - 2009-09-16

Company: https://www.keypedia.com/companies/cepheid/b8ab5e76-7447-435e-a3e3-c387ac1c40ec

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