FDA inspection

Maquet SAS: FDA inspection ending Feb 1, 2018

FDA inspection 1039724 · Voluntary Action Indicated (VAI) · Orleans Cedex 2

Key facts

Inspection ID 1039724
Firm Maquet SAS
FEI number 3002465150
Address Parc De Limere, Avenue De La Pomme De Pin
City Orleans Cedex 2
Country France
Fiscal year 2018
Inspection end date Feb 1, 2018
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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

Browse all FDA inspections