FDA inspection

Sumitomo Pharma America, Inc.: FDA inspection ending Nov 5, 2021

FDA inspection 1161579 · No Action Indicated (NAI) · Marlborough, MA

Key facts

Inspection ID 1161579
Firm Sumitomo Pharma America, Inc.
FEI number 1222021
Address 84 Waterford Dr
City Marlborough
State MA
ZIP 01752
Country United States
Fiscal year 2022
Inspection end date Nov 5, 2021
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
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
  • 10–99 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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