# BioCheck, Inc., South San Francisco, CA – FDA Inspections

Source: https://www.keypedia.com/companies/biocheck-inc/3c05ef75-fba1-42c8-b40b-24348534e385

> Inspection records and compliance data for BioCheck, Inc. in South San Francisco, California. 5 FDA inspections on record (1 OAI), last inspected February 07, 2023.

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## Details

- Name: BioCheck, Inc.
- FEI Number: 3002564473
- Address Line 1: 425 Eccles Ave
- City: South San Francisco
- State: California
- Zip Code: 94080
- Country Name: United States
- Address: 425 Eccles Ave, South San Francisco, California 94080, United States
- Country: United States

## Related Documents

- FDA Inspection 1204769 - BioCheck, Inc. - 2023-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2023
- FDA Inspection 1204769 - BioCheck, Inc. - 2023-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2023
- FDA Inspection 1060644 - BioCheck, Inc. - 2018-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2018
- FDA Inspection 1060644 - BioCheck, Inc. - 2018-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2018
- FDA Inspection 904632 - BioCheck, Inc. - 2014-12-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 12, 2014
- FDA Inspection 904632 - BioCheck, Inc. - 2014-12-12 — classification: No Action Indicated (NAI), source: FDA, date: December 12, 2014
- FDA Inspection 730360 - BioCheck, Inc. - 2011-06-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 17, 2011
- FDA Inspection 730360 - BioCheck, Inc. - 2011-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2011
- [FDA Inspection 665791 - BioCheck, Inc. - 2010-06-09](https://www.keypedia.com/records/fda_inspections/biocheck-inc/9051a2b0-a454-4c47-a5b2-585662568480) — classification: Official Action Indicated (OAI), source: FDA, date: June 9, 2010
- FDA Inspection 665791 - BioCheck, Inc. - 2010-06-09 — classification: Official Action Indicated (OAI), source: FDA, date: June 9, 2010

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