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FDA Inspection 745229 — Vitalant

Vitalant — FEI 2371456

The FDA completed an inspection of Vitalant on September 15, 2011 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
September 15, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, LA (United States)

Facility

Other inspections at this facility

  • 1231512 (NAI Thu Jul 11 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094101 (VAI Wed Jun 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993571 (NAI Tue Oct 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984244 (NAI Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 879849 (NAI Fri May 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources