FDA inspection

Dufner Instrumente GmbH: FDA inspection ending Mar 13, 2024

FDA inspection 1232698 · No Action Indicated (NAI) · Tuttlingen

Key facts

Inspection ID 1232698
Firm Dufner Instrumente GmbH
FEI number 3002806862
Address Fohrenstr. 9
City Tuttlingen
Country Germany
Fiscal year 2024
Inspection end date Mar 13, 2024
Classification No Action Indicated (NAI)
Project area Postmarket Assurance: 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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