FDA Inspection 1031323 — BioLIfe Plasma Services L.P.
The FDA completed an inspection of BioLIfe Plasma Services L.P. on October 12, 2017 in Dekalb, IL. 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 12, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Dekalb, IL (United States)