FDA inspection

ERCHINGER: FDA inspection ending Mar 5, 2015

FDA inspection 929018 · Voluntary Action Indicated (VAI) · Tuttlingen

Key facts

Inspection ID 929018
Firm ERCHINGER
FEI number 3002807421
Address Rudolf-Diesel-Str. 20
City Tuttlingen
Country Germany
Fiscal year 2015
Inspection end date Mar 5, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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