Company
United StatesCorneaGen - Richmond, Richmond, CA – FDA Inspections
Inspection records and compliance data for CorneaGen - Richmond in Richmond, California. 4 FDA inspections on record, last inspected May 31, 2018.
Company Profile
This profile covers CorneaGen - Richmond based in Richmond, California, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 1
- NAI
- 3
- Form 483s
- 0
- Warning letters
- 0
First inspected June 13, 2011. Last inspected May 31, 2018.
Most cited issue areas
- Documentation of CD testing and labs1 inspection
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 31, 2018 | NAI | Biologics · Blood and Blood Products | 1059878 |
| May 12, 2016 | NAI | Biologics · Human Cellular, Tissue, and Gene Therapies | 974353 |
| February 12, 2013 | NAI | Biologics · Human Cellular, Tissue, and Gene Therapies | 823345 |
| June 13, 2011 | VAI | Biologics · Human Cellular, Tissue, and Gene Therapies | 729194 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
CorneaGen - Richmond
FEI Number
3003449188
Address
880 Harbour Way S Ste 500, Richmond, California 94804, United States
Country
United States
ID: 75dc924b-7b44-4876-8e60-c6227fcf6bc4