FDA inspection

Allpack Group AG: FDA inspection ending Nov 6, 2009

FDA inspection 629336 · Voluntary Action Indicated (VAI) · Reinach BL

Key facts

Inspection ID 629336
Firm Allpack Group AG
FEI number 3004362706
Address Pfeffingerstrasse 45
City Reinach BL
Country Switzerland
Fiscal year 2010
Inspection end date Nov 6, 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