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/ Grifols USA, LLC
Grifols USA, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K113377
GLIADIN IGA AND GLIADIN LGA
December 14, 2012
K120169
INTERLAB IFE TEST USING G 26 VER. 2.0 INSTRUMENT
August 24, 2012
K102964
EU-TTG IGA AND EU-TTG IGG
March 7, 2011