# CorneaGen - Richmond – FDA Inspection, May 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/corneagen-richmond/78247ae5-77b6-4edd-a022-6a5d0698bed5
Source feed: FDA_Inspections

> FDA inspection 1059878 of CorneaGen - Richmond, May 31, 2018. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059878
- Company Name: CorneaGen - Richmond
- Inspection Date: 2018-05-31
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 974353 - 2016-05-12
- FDA Inspection 823345 - 2013-02-12
- [FDA Inspection 729194 - 2011-06-13](https://www.keypedia.com/records/fda_inspections/corneagen-richmond/7fefc635-1cbd-4d8e-afec-d941322c6b37)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roger-d-gawne/d2f40607-2408-45e3-a9f5-893d5bbe5b7e)

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

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