FDA Inspection 837107 — BioLife Plasma Services L.P.
The FDA completed an inspection of BioLife Plasma Services L.P. on June 19, 2013 in Muncie, IN. 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
- June 19, 2013
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Muncie, IN (United States)