FDA inspection

Regeneron Pharmaceuticals Inc: FDA inspection ending Feb 22, 2013

FDA inspection 819877 · Voluntary Action Indicated (VAI) · Tarrytown, NY

Key facts

Inspection ID 819877
Firm Regeneron Pharmaceuticals Inc
FEI number 1000521995
Address 777 Old Saw Mill River Rd
City Tarrytown
State NY
ZIP 10591
Country United States
Fiscal year 2013
Inspection end date Feb 22, 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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