FDA inspection

Eemagine Medical Imaging Solutions GmbH: FDA inspection ending Nov 30, 2017

FDA inspection 1032367 · Voluntary Action Indicated (VAI) · Berlin

Key facts

Inspection ID 1032367
Firm Eemagine Medical Imaging Solutions GmbH
FEI number 3003255845
Address Fabrik, Gubener Str. 47
City Berlin
Country Germany
Fiscal year 2018
Inspection end date Nov 30, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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