Home / Inspections / 990230

FDA Inspection 990230 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3007349296

The FDA completed an inspection of BioLife Plasma Services L.P. on October 18, 2016 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
October 18, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux City, IA (United States)

Facility

Other inspections at this facility

  • 1261469 (NAI Thu Jan 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1090778 (NAI Fri May 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 920248 (NAI Tue Mar 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 832021 (NAI Thu Apr 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 666770 (VAI Wed Jun 02 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources