FDA inspection

Synthes Zuchwil: FDA inspection ending Dec 16, 2016

FDA inspection 999721 · No Action Indicated (NAI) · Zuchwil

Key facts

Inspection ID 999721
Firm Synthes Zuchwil
FEI number 3009417901
Address Luzernstrasse 21
City Zuchwil
Country Switzerland
Fiscal year 2017
Inspection end date Dec 16, 2016
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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