FDA inspection

Selenium Medical S.A.S.: FDA inspection ending Sep 21, 2011

FDA inspection 749559 · No Action Indicated (NAI) · La Rochelle

Key facts

Inspection ID 749559
Firm Selenium Medical S.A.S.
FEI number 1000461041
Address Zone Industrielle Chef De Baie, 40 Rue Chef De Baie
City La Rochelle
Country France
Fiscal year 2011
Inspection end date Sep 21, 2011
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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