FDA inspection

Trokamed GmbH: FDA inspection ending Feb 19, 2016

FDA inspection 961048 · Voluntary Action Indicated (VAI) · Geisingen

Key facts

Inspection ID 961048
Firm Trokamed GmbH
FEI number 3004595684
Address Kleine Breite 17
City Geisingen
Country Germany
Fiscal year 2016
Inspection end date Feb 19, 2016
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No 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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