FDA Warning Letter — Interpharma Praha A.S.

Case 493758 — FEI 3002807299

The FDA took a Warning Letter action against Interpharma Praha A.S. on October 13, 2016 (Prague 12, Czech Republic). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Interpharma Praha A.S.
Date
October 13, 2016
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Prague 12 (Czech Republic)