FDA inspection

Somatex Medical Technologies GMBH: FDA inspection ending Sep 10, 2015

FDA inspection 941408 · No Action Indicated (NAI) · Berlin

Key facts

Inspection ID 941408
Firm Somatex Medical Technologies GMBH
FEI number 1000408433
Address Hohenzollerndamm 150/151
City Berlin
Country Germany
Fiscal year 2015
Inspection end date Sep 10, 2015
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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