FDA Inspection 1170411 — Maquet Cardiopulmonary Gmbh

Maquet Cardiopulmonary Gmbh — FEI 3009507273

The FDA completed an inspection of Maquet Cardiopulmonary Gmbh on April 28, 2022 in Rastatt. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Rastatt (Germany)