FDA inspection

IEM Gmbh: FDA inspection ending Oct 21, 2011

FDA inspection 753156 · Official Action Indicated (OAI) · Aachen

Key facts

Inspection ID 753156
Firm IEM Gmbh
FEI number 1000628323
Address Cockerillstr. 69
City Aachen
Country Germany
Fiscal year 2012
Inspection end date Oct 21, 2011
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 276156

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes 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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