FDA Inspection 830430 — Vitalant
The FDA completed an inspection of Vitalant on May 6, 2013 in Morgan City, 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
- May 6, 2013
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Morgan City, LA (United States)