FDA inspection

Smith & Nephew, Inc.: FDA inspection ending Aug 31, 2011

FDA inspection 743018 · Voluntary Action Indicated (VAI) · Saint Petersburg, FL

Key facts

Inspection ID 743018
Firm Smith & Nephew, Inc.
FEI number 3006760724
Address 970 Lake Carillon Dr Ste 110
City Saint Petersburg
State FL
ZIP 33716
Country United States
Fiscal year 2011
Inspection end date Aug 31, 2011
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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