FDA inspection

Aesku Group GmbH & Co. KG: FDA inspection ending Mar 2, 2017

FDA inspection 1008028 · Voluntary Action Indicated (VAI) · Wendelsheim

Key facts

Inspection ID 1008028
Firm Aesku Group GmbH & Co. KG
FEI number 3003825930
Address Mikro-forum-ring 2
City Wendelsheim
Country Germany
Fiscal year 2017
Inspection end date Mar 2, 2017
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

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