FDA inspection

BAK KOHLER Medical KG: FDA inspection ending Jan 19, 2012

FDA inspection 768246 · Voluntary Action Indicated (VAI) · Neuhausen Ob Eck Schwandor

Key facts

Inspection ID 768246
Firm BAK KOHLER Medical KG
FEI number 3005276402
Address Siemens-Ring 15
City Neuhausen Ob Eck Schwandor
Country Germany
Fiscal year 2012
Inspection end date Jan 19, 2012
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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