FDA inspection

Sofradim Production: FDA inspection ending Mar 19, 2015

FDA inspection 920587 · No Action Indicated (NAI) · Trevoux

Key facts

Inspection ID 920587
Firm Sofradim Production
FEI number 3003521774
Address 116 Avenue De Formans
City Trevoux
Country France
Fiscal year 2015
Inspection end date Mar 19, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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