FDA inspection

Rudischhauser Surgical Instruments Manufacturing GmbH: FDA inspection ending Dec 4, 2013

FDA inspection 859239 · Voluntary Action Indicated (VAI) · Tuttlingen

Key facts

Inspection ID 859239
Firm Rudischhauser Surgical Instruments Manufacturing GmbH
FEI number 3008237805
Address Gansacker 28
City Tuttlingen
Country Germany
Fiscal year 2014
Inspection end date Dec 4, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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