FDA inspection

Widex A/S: FDA inspection ending Nov 21, 2019

FDA inspection 1110943 · No Action Indicated (NAI) · Lynge

Key facts

Inspection ID 1110943
Firm Widex A/S
FEI number 3003557127
Address Nymollevej 6
City Lynge
Country Denmark
Fiscal year 2020
Inspection end date Nov 21, 2019
Classification No Action Indicated (NAI)
Project area Compliance: 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

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