Home / Inspections / 748170

FDA Inspection 748170 — Prothya Biosolutions Netherlands B.V.

Prothya Biosolutions Netherlands B.V. — FEI 3007166802

The FDA completed an inspection of Prothya Biosolutions Netherlands B.V. on September 28, 2011 in Amsterdam. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Amsterdam (Netherlands)

Facility

Other inspections at this facility

  • 1046705 (VAI Fri Mar 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969120 (VAI Fri May 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906173 (OAI Thu Nov 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835110 (OAI Tue Jun 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 620661 (VAI Tue Sep 15 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources