FDA inspection

Medart A /S: FDA inspection ending Sep 13, 2013

FDA inspection 849997 · Voluntary Action Indicated (VAI) · Hvidovre

Key facts

Inspection ID 849997
Firm Medart A /S
FEI number 3005616124
Address Industriholmen 15A
City Hvidovre
Country Denmark
Fiscal year 2013
Inspection end date Sep 13, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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