FDA inspection

Sumitomo Pharma America, Inc.: FDA inspection ending May 24, 2013

FDA inspection 843011 · Voluntary Action Indicated (VAI) · Marlborough, MA

Key facts

Inspection ID 843011
Firm Sumitomo Pharma America, Inc.
FEI number 1222021
Address 84 Waterford Dr
City Marlborough
State MA
ZIP 01752
Country United States
Fiscal year 2013
Inspection end date May 24, 2013
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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