FDA Warning Letter — Teoxane S.A.

Case 391672 — FEI 3005975625

The FDA took a Warning Letter action against Teoxane S.A. on April 19, 2013 (Geneva, Switzerland). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Teoxane S.A.
Date
April 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Geneva (Switzerland)