FDA inspection

Maquet SAS: FDA inspection ending Feb 7, 2013

FDA inspection 819201 · No Action Indicated (NAI) · Orleans Cedex 2

Key facts

Inspection ID 819201
Firm Maquet SAS
FEI number 3002465150
Address Parc De Limere, Avenue De La Pomme De Pin
City Orleans Cedex 2
Country France
Fiscal year 2013
Inspection end date Feb 7, 2013
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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