# CorneaGen - Richmond - Inspection Records

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

> Inspection records and compliance data for CorneaGen - Richmond in Richmond, California. Access full analysis and detailed observations.

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## Details

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

## 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](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/509a259e-e017-496b-ba11-480c6232fb49) — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2018
- [FDA Inspection 974353 - CorneaGen - Richmond - 2016-05-12](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/22f5740d-53c5-42f6-aecd-5164bb2ce585) — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2016
- [FDA Inspection 823345 - CorneaGen - Richmond - 2013-02-12](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/6378d570-ee2b-4052-a9c9-f506433a31f1) — 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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