FDA Inspection 979670 — BioLife Plasma Services L.P.
The FDA completed an inspection of BioLife Plasma Services L.P. on Aug 1, 2016 in Ankeny, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 1, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Ankeny, IA (United States)