FDA inspection

Rudischhauser Surgical Instruments Manufacturing GmbH: FDA inspection ending Dec 8, 2016

FDA inspection 995720 · Voluntary Action Indicated (VAI) · Tuttlingen

Key facts

Inspection ID 995720
Firm Rudischhauser Surgical Instruments Manufacturing GmbH
FEI number 3008237805
Address Gansacker 28
City Tuttlingen
Country Germany
Fiscal year 2017
Inspection end date Dec 8, 2016
Classification Voluntary Action Indicated (VAI)
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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