FDA Warning Letter — Stephanix

Case 429819 — FEI 3006972752

The FDA took a Warning Letter action against Stephanix on August 12, 2016 (La Ricamarie, France). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Stephanix
Date
August 12, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
La Ricamarie (France)