FDA inspection

Regeneron Pharmaceuticals Inc: FDA inspection ending Feb 5, 2016

FDA inspection 965332 · No Action Indicated (NAI) · Rensselaer, NY

Key facts

Inspection ID 965332
Firm Regeneron Pharmaceuticals Inc
FEI number 1000514603
Address 81 Columbia Tpke
City Rensselaer
State NY
ZIP 12144-3411
Fiscal year 2016
Inspection end date Feb 5, 2016
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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