FDA Warning Letter — DCA, Inc.

Case 525833 — FEI 3005823862

The FDA took a Warning Letter action against DCA, Inc. on Jun 1, 2017 (Southington, CT). The action was issued by CDER and concerns drugs products.

Action Details

Facility
DCA, Inc.
Date
Jun 1, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Southington, CT (United States)