# FDA Inspection 894961 - SightLife/CorneaGen - September 11, 2014

Source: https://www.keypedia.com/records/fda_inspections/sightlifecorneagen/72b8ae40-cc52-446b-9fb9-a0500a552dbc
Source feed: FDA_Inspections

> FDA Inspection 894961 for SightLife/CorneaGen on September 11, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894961
- Company Name: SightLife/CorneaGen
- Inspection Date: 2014-09-11
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/sightlifecorneagen/893bd611-bd46-4e4d-bf08-6d9a6272be74

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