Compliance document

Form FDA 483: Daiichi Sankyo Co., Ltd.

FDA FOIA

Key facts

Document type Form FDA 483
Firm Daiichi Sankyo Co., Ltd.
FEI number 3006222711
Inspection 490874
Collection FDA FOIA

At a glance

  • 10–99 Pages
  • 1–9 FDA inspections at this FEI

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

About FDA inspection and compliance documents

The Orca1 document library indexes FDA compliance documents such as Form 483 observations, establishment inspection reports and firm responses. Documents are available to Orca1 subscribers only.

Source: U.S. Food and Drug Administration (FDA) records, Orca1 document library

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