FDA inspection

Vincent Systems Gmbh: FDA inspection ending Jan 21, 2016

FDA inspection 962772 · Voluntary Action Indicated (VAI) · Karlsruhe

Key facts

Inspection ID 962772
Firm Vincent Systems Gmbh
FEI number 3007727466
Address Breite Str. 155
City Karlsruhe
Country Germany
Fiscal year 2016
Inspection end date Jan 21, 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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