FDA Warning Letter — Herniamesh S.r.l

Case 480085 — FEI 3005404334

The FDA took a Warning Letter action against Herniamesh S.r.l on November 23, 2015 (Chivasso, Italy). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Herniamesh S.r.l
Date
November 23, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Chivasso (Italy)