FDA inspection

Askion Gmbh: FDA inspection ending Jan 31, 2013

FDA inspection 819842 · Voluntary Action Indicated (VAI) · Gera

Key facts

Inspection ID 819842
Firm Askion Gmbh
FEI number 3007055152
Address Gewerbepark Keplerstr. 17-19
City Gera
Country Germany
Fiscal year 2013
Inspection end date Jan 31, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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