FDA inspection

MediTop Bv: FDA inspection ending Sep 10, 2015

FDA inspection 943699 · Voluntary Action Indicated (VAI) · Montfoort

Key facts

Inspection ID 943699
Firm MediTop Bv
FEI number 3006581122
Address Vlasakker 22
City Montfoort
Country Netherlands
Fiscal year 2015
Inspection end date Sep 10, 2015
Classification Voluntary Action Indicated (VAI)
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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