FDA Warning Letter — Homeolab USA Inc.

Case 398217 — FEI 1000399435

The FDA took a Warning Letter action against Homeolab USA Inc. on September 19, 2013 (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
September 19, 2013
Fiscal Year
2013
Product Type
Drugs
Center
CDER
Location
Montreal (Canada)