FDA inspection

Tutogen Medical GmbH: FDA inspection ending Sep 23, 2015

FDA inspection 943795 · No Action Indicated (NAI) · Neunkirchen A. Brand

Key facts

Inspection ID 943795
Firm Tutogen Medical GmbH
FEI number 3002924436
Address Neunkirchen am Brand, Industriestr. 6
City Neunkirchen A. Brand
Country Germany
Fiscal year 2015
Inspection end date Sep 23, 2015
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

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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