FDA Inspection 854366 — Maquet Critical Care AB

Maquet Critical Care AB — FEI 3002808128

The FDA completed an inspection of Maquet Critical Care AB on September 13, 2013 in Solna. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

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