FDA inspection

Smith & Nephew Orthopaedics GmbH: FDA inspection ending Feb 22, 2013

FDA inspection 823996 · No Action Indicated (NAI) · Tuttlingen

Key facts

Inspection ID 823996
Firm Smith & Nephew Orthopaedics GmbH
FEI number 3002465897
Address Alemannenstr. 14
City Tuttlingen
Country Germany
Fiscal year 2013
Inspection end date Feb 22, 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
  • 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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