FDA Inspection 1029767 — CorneaGen, LLC
The FDA completed an inspection of CorneaGen, LLC on Oct 20, 2017 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 20, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Irvine, CA (United States)