FDA Warning Letter — Homeocare Laboratories, Inc.

Case 521717 — FEI 3008420443

The FDA took a Warning Letter action against Homeocare Laboratories, Inc. on September 7, 2017 (Yonkers, NY). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Homeocare Laboratories, Inc.
Date
September 7, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Yonkers, NY (United States)