FDA Warning Letter — Interquim S.A.

Case 507036 — FEI 3002807304

The FDA took a Warning Letter action against Interquim S.A. on November 22, 2016 (Sant Cugat Del Valles, Spain). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Interquim S.A.
Date
November 22, 2016
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Sant Cugat Del Valles (Spain)