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FDA Inspection 1098545 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 2575934

The FDA completed an inspection of Vitalant Reference and Transfusion Service on August 1, 2019 in Pittsburgh, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 1, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Citations

IDCFRDescription
3521 CFR 606.40Clean & orderly

Facility

Other inspections at this facility

  • 992485 (VAI Thu Nov 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904557 (NAI Thu Oct 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 807457 (NAI Fri Nov 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 695926 (NAI Fri Oct 29 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 553165 (NAI Mon Nov 24 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources