FDA inspection

LeMaitre Vascular, Inc.: FDA inspection ending Jan 25, 2013

FDA inspection 816080 · No Action Indicated (NAI) · North Brunswick, NJ

Key facts

Inspection ID 816080
Firm LeMaitre Vascular, Inc.
FEI number 1000121696
Address 206 N Center Dr # 208
City North Brunswick
State NJ
ZIP 08902
Country United States
Fiscal year 2013
Inspection end date Jan 25, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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