FDA Inspection 1021570 — BioMerieux SA

BioMerieux SA — FEI 1000611339

The FDA completed an inspection of BioMerieux SA on Jun 22, 2017 in Marcy L'Etoile. 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
Jun 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Marcy L'Etoile (France)

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