FDA Inspection 1258668 — Maquet SAS

Maquet SAS — FEI 3002465150

The FDA completed an inspection of Maquet SAS on Jan 16, 2025 in Orleans Cedex 2. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Orleans Cedex 2 (France)

Citations

IDCFRDescription
316021 CFR 820.184Lack of or inadequate DHR procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

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