FDA inspection

Enraf-Nonius B.V.: FDA inspection ending Apr 2, 2015

FDA inspection 923892 · No Action Indicated (NAI) · Rotterdam

Key facts

Inspection ID 923892
Firm Enraf-Nonius B.V.
FEI number 3002806913
Address Vareseweg 127
City Rotterdam
Country Netherlands
Fiscal year 2015
Inspection end date Apr 2, 2015
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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