FDA inspection

TEM INNOVATIONS GMBH: FDA inspection ending May 31, 2016

FDA inspection 975619 · No Action Indicated (NAI) · Munich

Key facts

Inspection ID 975619
Firm TEM INNOVATIONS GMBH
FEI number 3005792925
Address Martin-kollar-str. 13
City Munich
Country Germany
Fiscal year 2016
Inspection end date May 31, 2016
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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