# FDA Inspection 1061992 - CorneaGen Inc. - July 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/6319f14a-8037-434b-b4c1-17288fdbe7f9
Source feed: FDA_Inspections

> FDA Inspection 1061992 for CorneaGen Inc. on July 20, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1061992
- Company Name: CorneaGen Inc.
- Inspection Date: 2018-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1207713 - 2023-05-31](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/9546350a-520a-418e-9e0c-472996e1ca70)
- [FDA Inspection 1207713 - 2023-05-31](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/a5146096-70a5-4e18-b1d1-ad5e2643b3e7)
- [FDA Inspection 1149011 - 2021-07-14](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/29d8d155-afb4-4305-bce4-120aba4772b2)
- [FDA Inspection 946041 - 2015-10-22](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/9b015230-b63c-4da3-a8e3-09d62c7792d7)
- [FDA Inspection 870037 - 2014-02-28](https://www.globalkeysolutions.net/records/fda_inspections/corneagen-inc/61c610b6-38c6-4483-8e1d-0d32b33bff12)

Company: https://www.globalkeysolutions.net/companies/corneagen-inc/63b0f20d-2789-4c29-90c7-251cd951234a

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d