FDA Warning Letter — Eurotrol B.V.

Case 433999 — FEI 3005695774

The FDA took a Warning Letter action against Eurotrol B.V. on Nov 19, 2014 (Ede Gld, Netherlands). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
Eurotrol B.V.
Date
Nov 19, 2014
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Ede Gld (Netherlands)

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