FDA Inspection 917411 — MEDICOAT SAS

MEDICOAT SAS — FEI 3007120646

The FDA completed an inspection of MEDICOAT SAS on Feb 12, 2015 in Etupes. 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
Feb 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Etupes (France)

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