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FDA Inspection 1058488 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3003908509

The FDA completed an inspection of BioLife Plasma Services L.P. on June 19, 2018 in Cheyenne, WY. 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, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cheyenne, WY (United States)

Facility

Other inspections at this facility

  • 1272389 (NAI Thu May 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 947669 (NAI Wed Sep 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850245 (NAI Thu Sep 26 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources