# CorneaGen - Richmond, Richmond, CA – FDA Inspections

Source: https://www.keypedia.com/companies/corneagen-richmond/75dc924b-7b44-4876-8e60-c6227fcf6bc4

> Inspection records and compliance data for CorneaGen - Richmond in Richmond, California. 4 FDA inspections on record, last inspected May 31, 2018.

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## Details

- Name: CorneaGen - Richmond
- FEI Number: 3003449188
- Address Line 1: 880 Harbour Way S Ste 500
- City: Richmond
- State: California
- Zip Code: 94804
- Country Name: United States
- Address: 880 Harbour Way S Ste 500, Richmond, California 94804, United States
- Country: United States

## Related Documents

- [FDA Inspection 1059878 - CorneaGen - Richmond - 2018-05-31](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/78247ae5-77b6-4edd-a022-6a5d0698bed5) — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2018
- FDA Inspection 1059878 - CorneaGen - Richmond - 2018-05-31 — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2018
- FDA Inspection 974353 - CorneaGen - Richmond - 2016-05-12 — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2016
- FDA Inspection 823345 - CorneaGen - Richmond - 2013-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2013
- [FDA Inspection 729194 - CorneaGen - Richmond - 2011-06-13](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/7fefc635-1cbd-4d8e-afec-d941322c6b37) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2011

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