FDA inspection

Perouse Medical: FDA inspection ending Nov 21, 2013

FDA inspection 857492 · Official Action Indicated (OAI) · Irigny

Key facts

Inspection ID 857492
Firm Perouse Medical
FEI number 3004160911
Address 135 Route Neuve
City Irigny
Country France
Fiscal year 2014
Inspection end date Nov 21, 2013
Classification Official Action Indicated (OAI)
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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