FDA Warning Letter — Homeolab USA Inc.

Case 523072 — FEI 1000399435

The FDA took a Warning Letter action against Homeolab USA Inc. on August 2, 2017 (Montreal, Canada). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Homeolab USA Inc.
Date
August 2, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Montreal (Canada)