FDA inspection

Dottikon Exclusive Synthesis AG: FDA inspection ending Jul 14, 2017

FDA inspection 1018903 · Voluntary Action Indicated (VAI) · Dottikon

Key facts

Inspection ID 1018903
Firm Dottikon Exclusive Synthesis AG
FEI number 3002806909
Address Hembrunnstrasse 17
City Dottikon
Country Switzerland
Fiscal year 2017
Inspection end date Jul 14, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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