FDA inspection

MEDICAMAT S.A.: FDA inspection ending Oct 16, 2012

FDA inspection 805625 · Voluntary Action Indicated (VAI) · Malakoff

Key facts

Inspection ID 805625
Firm MEDICAMAT S.A.
FEI number 3002642065
Address 59 Avenue Augustin Dumont
City Malakoff
Country France
Fiscal year 2013
Inspection end date Oct 16, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices
Warning letter 391311

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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