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FDA Inspection 604691 — Grifols Biomat

Grifols Biomat — FEI 3002717772

The FDA completed an inspection of Grifols Biomat on August 13, 2009 in Reading, PA. 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
August 13, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Reading, PA (United States)

Facility

Other inspections at this facility

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  • 1014326 (NAI Thu May 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 930547 (NAI Thu Jun 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835676 (NAI Wed Jun 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 739338 (NAI Fri Aug 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources