FDA Inspection 1170411 — Maquet Cardiopulmonary Gmbh

Maquet Cardiopulmonary Gmbh — FEI 3009507273

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

Inspection details

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

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