FDA Inspection 1107221 — BioLife Plasma Services LP
The FDA completed an inspection of BioLife Plasma Services LP on October 11, 2019 in West des Moines, IA. 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 11, 2019
- Fiscal Year
- 2020
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- West des Moines, IA (United States)