FDA inspection

LDR Medical: FDA inspection ending Jul 9, 2009

FDA inspection 600305 · Voluntary Action Indicated (VAI) · Sainte-Savine Aube

Key facts

Inspection ID 600305
Firm LDR Medical
FEI number 3004788213
Address Hotel de Bureaux 1, 4 rue Gustave Eiffel
City Sainte-Savine Aube
Country France
Fiscal year 2009
Inspection end date Jul 9, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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