FDA Inspection 985034 — Genvion Corporation
The FDA completed an inspection of Genvion Corporation on June 17, 2016 in Winnipeg. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 17, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Winnipeg (Canada)