FDA Warning Letter — Aplicare Products, LLC

Case 489281 — FEI 1220701

The FDA took a Warning Letter action against Aplicare Products, LLC on December 15, 2016 (Meriden, CT). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Aplicare Products, LLC
Date
December 15, 2016
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Meriden, CT (United States)