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FDA Inspection 882156 — Daiichi Sankyo Europe GmbH

Daiichi Sankyo Europe GmbH — FEI 3003282622

The FDA completed an inspection of Daiichi Sankyo Europe GmbH on May 15, 2014 in Pfaffenhofen A.D.Ilm. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 15, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pfaffenhofen A.D.Ilm (Germany)

Facility

Other inspections at this facility

  • 1275919 (VAI Fri Jul 18 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073797 (NAI Fri Oct 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 802508 (NAI Thu Sep 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 649526 (NAI Fri Jan 29 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

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