FDA inspection

SenTec AG: FDA inspection ending Oct 25, 2012

FDA inspection 816129 · No Action Indicated (NAI) · Therwil

Key facts

Inspection ID 816129
Firm SenTec AG
FEI number 3004149774
Address Ringstrasse 39
City Therwil
Country Switzerland
Fiscal year 2013
Inspection end date Oct 25, 2012
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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