FDA inspection

Kettenbach GmbH & Co. KG: FDA inspection ending Jun 7, 2007

FDA inspection 477365 · Voluntary Action Indicated (VAI) · Eschenburg

Key facts

Inspection ID 477365
Firm Kettenbach GmbH & Co. KG
FEI number 3006349398
Address Im Heerfeld 7
City Eschenburg
Fiscal year 2007
Inspection end date Jun 7, 2007
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med 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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