FDA inspection

Smith & Nephew, Inc.: FDA inspection ending Dec 8, 2015

FDA inspection 960574 · Voluntary Action Indicated (VAI) · Mansfield, MA

Key facts

Inspection ID 960574
Firm Smith & Nephew, Inc.
FEI number 1219602
Address 130 & 120 Forbes Blvd
City Mansfield
State MA
ZIP 02048
Country United States
Fiscal year 2016
Inspection end date Dec 8, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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
  • 1–9 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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