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FDA Warning Letter — Teoxane S.A.

Case 391672 — FEI 3005975625

The FDA took a Warning Letter action against Teoxane S.A. on Apr 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
Apr 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Geneva (Switzerland)

Facility

Recent inspections

FDA data resources

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