# CorneaGen - Inspection Records

Source: https://www.keypedia.com/companies/corneagen/9df61303-9794-4f51-935f-2f9a2bfe1945

> Inspection records and compliance data for CorneaGen in Baltimore, Maryland. Access full analysis and detailed observations.

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## Details

- Name: CorneaGen
- FEI Number: 3001236461
- City: Baltimore
- State: Maryland
- Country Name: United States
- Address Line 1: 5520 Research Park Dr Ste 400
- Zip Code: 21228

## Related Documents

- [FDA Inspection 1153003 - CorneaGen - 2021-09-15](https://www.keypedia.com/records/fda_inspections/corneagen/eee66bf9-8001-4fdf-bf4e-d3de36d0996d) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2021
- [FDA Inspection 1153003 - CorneaGen - 2021-09-15](https://www.keypedia.com/records/fda_inspections/corneagen/4ebb177e-01d2-497c-96a7-efdb0d1a6bf0) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2021
- [FDA Inspection 1068567 - CorneaGen - 2018-09-14](https://www.keypedia.com/records/fda_inspections/corneagen/4260b9bc-5ad1-4be7-a9d8-a5769d9ac8c5) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2018
- [FDA Inspection 981338 - CorneaGen - 2016-08-22](https://www.keypedia.com/records/fda_inspections/corneagen/f2f0a1a7-8206-454e-9926-5dfa45e07f57) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2016
- [FDA Inspection 872226 - CorneaGen - 2014-03-25](https://www.keypedia.com/records/fda_inspections/corneagen/2c0f1f03-25f5-4798-a087-d14ca3e73abc) — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2014
- [FDA Inspection 807888 - CorneaGen - 2012-11-16](https://www.keypedia.com/records/fda_inspections/corneagen/855aee47-9ee4-4189-ad09-e247f710ad45) — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2012
- [FDA Inspection 666742 - CorneaGen - 2010-06-09](https://www.keypedia.com/records/fda_inspections/corneagen/e824f745-6867-412d-a8e5-edd541ae262b) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- [FDA Inspection 638570 - CorneaGen - 2010-01-21](https://www.keypedia.com/records/fda_inspections/corneagen/a9192218-a310-4883-921c-df2c59fbf62f) — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2010

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