FDA inspection

Daiichi Sankyo Altkirch: FDA inspection ending Apr 22, 2016

FDA inspection 969549 · No Action Indicated (NAI) · Altkirch

Key facts

Inspection ID 969549
Firm Daiichi Sankyo Altkirch
FEI number 3001400724
Address Daiichi Sankyo Altkirch Sarl, 39 Rue Du 3e Zouave; Bp 60005
City Altkirch
Country France
Fiscal year 2016
Inspection end date Apr 22, 2016
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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