FDA inspection

Medistri SA: FDA inspection ending Jan 31, 2019

FDA inspection 1087831 · No Action Indicated (NAI) · Domdidier

Key facts

Inspection ID 1087831
Firm Medistri SA
FEI number 3006946276
Address Route De L'Industrie 96, Case Postale 115
City Domdidier
Country Switzerland
Fiscal year 2019
Inspection end date Jan 31, 2019
Classification No Action Indicated (NAI)
Project area Project Evaluation: Devices
Product type Devices

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

Browse all FDA inspections