FDA Inspection 1090778 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3007349296

The FDA completed an inspection of BioLife Plasma Services L.P. on May 17, 2019 in Sioux City, 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
May 17, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux City, IA (United States)