FDA Inspection 993571 — Vitalant
The FDA completed an inspection of Vitalant on October 25, 2016 in Lafayette, LA. 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
- October 25, 2016
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lafayette, LA (United States)