FDA Inspection 982339 — Vitalant
The FDA completed an inspection of Vitalant on Aug 10, 2016 in Cheyenne, WY. 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
- Aug 10, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Cheyenne, WY (United States)