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FDA Inspection 1038349 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 1627981

The FDA completed an inspection of BioLife Plasma Services, L.P. on January 10, 2018 in Denton, TX. 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
January 10, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Denton, TX (United States)

Facility

Other inspections at this facility

  • 1153743 (NAI Thu Sep 23 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 945062 (NAI Thu Oct 08 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 844418 (NAI Fri Aug 09 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 706154 (NAI Tue Jan 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources