FDA inspection

Askion Gmbh: FDA inspection ending Sep 3, 2009

FDA inspection 623328 · Voluntary Action Indicated (VAI) · Gera

Key facts

Inspection ID 623328
Firm Askion Gmbh
FEI number 3007055152
Address Gewerbepark Keplerstr. 17-19
City Gera
Country Germany
Fiscal year 2009
Inspection end date Sep 3, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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

Browse all FDA inspections