FDA inspection

SPINEVISION SAS: FDA inspection ending Mar 15, 2012

FDA inspection 773258 · No Action Indicated (NAI) · Antony

Key facts

Inspection ID 773258
Firm SPINEVISION SAS
FEI number 3003526896
Address Batiment C E Batiment E
City Antony
Country France
Fiscal year 2012
Inspection end date Mar 15, 2012
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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