FDA inspection

Sofradim Production: FDA inspection ending Nov 7, 2011

FDA inspection 752368 · Voluntary Action Indicated (VAI) · Trevoux

Key facts

Inspection ID 752368
Firm Sofradim Production
FEI number 3003521774
Address 116 Avenue De Formans
City Trevoux
Country France
Fiscal year 2012
Inspection end date Nov 7, 2011
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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