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FDA Inspection 870037 — CorneaGen Inc.

CorneaGen Inc. — FEI 3005357288

The FDA completed an inspection of CorneaGen Inc. on February 28, 2014 in Winston Salem, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 28, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Winston Salem, NC (United States)

Facility

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FDA data resources