FDA Inspection 854366 — Maquet Critical Care AB

Maquet Critical Care AB — FEI 3002808128

The FDA completed an inspection of Maquet Critical Care AB on Sep 13, 2013 in Solna. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Sep 13, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Solna (Sweden)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.