FDA Warning Letter — TMS International

Case 379460 — FEI 3006071260

The FDA took a Warning Letter action against TMS International on Dec 13, 2012 (Oldenzaal, Netherlands). The action was issued by CDRH and concerns devices products.

Action Details

Facility
TMS International
Date
Dec 13, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Oldenzaal (Netherlands)

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