FDA inspection

IEM Gmbh: FDA inspection ending Jan 24, 2013

FDA inspection 818868 · No Action Indicated (NAI) · Aachen

Key facts

Inspection ID 818868
Firm IEM Gmbh
FEI number 1000628323
Address Cockerillstr. 69
City Aachen
Country Germany
Fiscal year 2013
Inspection end date Jan 24, 2013
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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