FDA Inspection 1038442 — Medtech SAS

Medtech SAS — FEI 3009185973

The FDA completed an inspection of Medtech SAS on November 16, 2017 in Mauguio. 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
November 16, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Mauguio (France)