FDA Warning Letter — TYTEX SLOVAKIA S.R.O.

Case 395556 — FEI 3006121457

The FDA took a Warning Letter action against TYTEX SLOVAKIA S.R.O. on June 12, 2013 (Humenne, Slovakia). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
TYTEX SLOVAKIA S.R.O.
Date
June 12, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Humenne (Slovakia)