FDA Warning Letter — Interlab S.r.l.

Case 392347 — FEI 3003961883

The FDA took a Warning Letter action against Interlab S.r.l. on February 28, 2013 (Rome, Italy). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Interlab S.r.l.
Date
February 28, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Rome (Italy)