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FDA Inspection 960885 — Grifols Diagnostic Solutions, INC.

Grifols Diagnostic Solutions, INC. — FEI 3003460312

The FDA completed an inspection of Grifols Diagnostic Solutions, INC. on January 18, 2016 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 18, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1279554 (VAI Tue Aug 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1162488 (VAI Thu Feb 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1076855 (NAI Mon Dec 10 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037913 (NAI Thu Nov 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 977390 (NAI Thu Jun 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources