FDA Inspection 974353 — CorneaGen - Richmond
The FDA completed an inspection of CorneaGen - Richmond on May 12, 2016 in Richmond, 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
- May 12, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Richmond, CA (United States)