# Cepheid, Sunnyvale, CA – FDA Inspections

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

> Inspection records and compliance data for Cepheid in Sunnyvale, California. 5 FDA inspections on record, last inspected August 09, 2017.

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## Details

- Name: Cepheid
- FEI Number: 3004530258
- Address Line 1: 904 E Caribbean Dr
- City: Sunnyvale
- State: California
- Zip Code: 94089
- Country Name: United States
- Address: 904 E Caribbean Dr, Sunnyvale, California 94089, United States
- Country: United States

## Related Documents

- FDA Inspection 1026773 - Cepheid - 2017-08-09 — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2017
- FDA Inspection 1026773 - Cepheid - 2017-08-09 — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2017
- FDA Inspection 928802 - Cepheid - 2015-06-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 16, 2015
- [FDA Inspection 928802 - Cepheid - 2015-06-16](https://www.keypedia.com/records/fda_inspections/cepheid/da35e071-bda6-4198-8e8a-7f2abbcf740c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 16, 2015
- FDA Inspection 763635 - Cepheid - 2012-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2012
- FDA Inspection 763635 - Cepheid - 2012-01-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2012
- FDA Inspection 695802 - Cepheid - 2010-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2010
- [FDA Inspection 695802 - Cepheid - 2010-10-29](https://www.keypedia.com/records/fda_inspections/cepheid/c7096018-7f22-4e9e-837c-29fca4c4b4e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2010
- FDA Inspection 612704 - Cepheid - 2009-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2009
- FDA Inspection 612704 - Cepheid - 2009-09-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2009

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