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FDA Inspection 565003 — Our Lady of Lourdes Blood Donor Center

Our Lady of Lourdes Blood Donor Center — FEI 3005224112

The FDA completed an inspection of Our Lady of Lourdes Blood Donor Center on February 25, 2009 in Lafayette, LA. 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
February 25, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, LA (United States)

Facility

Other inspections at this facility

  • 1204962 (NAI Wed Mar 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044580 (NAI Thu Feb 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 937843 (NAI Thu Jul 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources