# CorneaGen, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/corneagen-inc/57206953-05f1-4b04-8917-be34f14885c3

> Inspection records and compliance data for CorneaGen, Inc. in South San Francisco, California. Access full analysis and detailed observations.

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## Details

- Name: CorneaGen, Inc.
- FEI Number: 3009122697
- City: South San Francisco
- State: California
- Country Name: United States
- Address Line 1: 6000 Shoreline Ct Ste 202
- Zip Code: 94080

## Related Documents

- [FDA Inspection 1282090 - CorneaGen, Inc. - 2025-09-10](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/26db1cc8-47a4-4a64-85e9-283c66b1143b) — source: FDA, date: September 10, 2025
- [FDA Inspection 1282090 - CorneaGen, Inc. - 2025-09-10](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/b5d07caf-b9a0-4d0f-bc82-64b95be99de2) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2025
- [483 - CorneaGen, Inc. - 2022-07-29](https://www.globalkeysolutions.net/records/483/corneagen-inc/b55b1715-158f-460d-a5f4-947987c7ca2e) — source: FDA, date: July 29, 2022
- [FDA Inspection 1176014 - CorneaGen, Inc. - 2022-07-29](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/0201d817-ccbe-4bb1-9e8f-206c099898f3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 29, 2022
- [FDA Inspection 1047476 - CorneaGen, Inc. - 2018-02-27](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/eefa8239-a326-4445-b57d-1431050a3edb) — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2018
- [FDA Inspection 977565 - CorneaGen, Inc. - 2016-06-15](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/134fd718-00a2-40fe-82d3-32a116632cc5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2016
- [FDA Inspection 836377 - CorneaGen, Inc. - 2013-06-17](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/70266549-6fb8-4dad-a3eb-91b42632b947) — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2013

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- [investigator](https://www.globalkeysolutions.net/people/ka-l-wong/e624263d-e2c0-4b80-b5d9-ea84e29baa6b)