FDA inspection

Smith & Nephew, Inc.: FDA inspection ending Nov 26, 2013

FDA inspection 858923 · Official Action Indicated (OAI) · Saint Petersburg, FL

Key facts

Inspection ID 858923
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 2014
Inspection end date Nov 26, 2013
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 418706

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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