# CorneaGen, Baltimore, MD – FDA Inspections

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

> Inspection records and compliance data for CorneaGen in Baltimore, Maryland. 8 FDA inspections on record, last inspected September 22, 2026.

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## Details

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

## Related Documents

- FDA Inspection 1338912 - CorneaGen - 2026-09-22 — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2026
- FDA Inspection 1153003 - CorneaGen - 2021-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2021
- FDA Inspection 1153003 - CorneaGen - 2021-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2021
- FDA Inspection 1068567 - CorneaGen - 2018-09-14 — 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 — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2014
- FDA Inspection 807888 - CorneaGen - 2012-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2012
- FDA Inspection 666742 - CorneaGen - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- FDA Inspection 638570 - CorneaGen - 2010-01-21 — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2010

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